Variant #0000557499 (NC_000016.9:g.223122A>G, NC_000016.9(NM_000517.4):c.96-2A>G (HBA2))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.223122A>G
DNA change (hg38) g.173123A>G
Published as HBA2(NM_000517.4):c.96-2A>G (p.?), HBA2(NM_000517.6):c.96-2A>G
ISCN -
DB-ID HBA2_000496 See all 6 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
HBA2 NM_000517.4 +/. - c.96-2A>G - r.spl? p.?
HBA1 NM_000558.3 +/. - c.-3594A>G - r.(?) p.(=)


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