Variant #0000288957 (NC_000016.9:g.223008_223012del, NC_000016.9(NM_000517.4):c.95+2_95+6del (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.223008_223012del
DNA change (hg38) g.173009_173013del
Published as HBA2(NM_000517.6):c.95+2_95+6delTGAGG
ISCN -
DB-ID HBA2_004006
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-07 11:13:32 +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.95+2_95+6del - r.spl? p.?
HBA1 NM_000558.3 +/. - c.-3708_-3704del - r.(?) p.(=)


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