Canonical Allele Identifier: CA375686792

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136132922C>T (hg19) ; chr9:g.133257535C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133257535C>T , CM000671.2:g.133257535C>T	GRCh38
NC_000009.11:g.136132922C>T , CM000671.1:g.136132922C>T	GRCh37
NC_000009.10:g.135122743C>T	NCBI36
NG_006669.1:g.20132G>A
NG_006669.2:g.22680G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.277G>A
ENST00000647353.1:n.54-6383G>A
ENST00000651471.1:n.329+507G>A
ENST00000679909.1:c.28+17627G>A	ENSP00000506089.1:n.28+17627G>A
ENST00000453660.3:n.259G>A
ENST00000538324.2:c.247G>A	ENSP00000483018.1:p.Asp83Asn
ENST00000611156.4:c.247G>A	ENSP00000483265.1:p.Asp83Asn
NM_020469.2:c.247G>A	NP_065202.2:p.Asp83Asn
NM_020469.3:c.247G>A	NP_065202.2:p.Asp83Asn