Variant #0000288948 (NC_000016.9:g.226927G>A, NM_000517.4:c.*3328G>A (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.226927G>A
DNA change (hg38) g.176928G>A
Published as HBA1(NM_000558.5):c.96-1G>A
ISCN -
DB-ID HBA1_003001
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) 0.00019 View details
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 11:26:04 +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.*3328G>A - r.(=) p.(=)
HBA1 NM_000558.3 +/. - c.96-1G>A - r.spl? p.?
HBQ1 NM_005331.4 +/. - c.-3559G>A - r.(?) p.(=)


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