Canonical Allele Identifier: CA375686628

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136132845A>T (hg19) ; chr9:g.133257458A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133257458A>T , CM000671.2:g.133257458A>T	GRCh38
NC_000009.11:g.136132845A>T , CM000671.1:g.136132845A>T	GRCh37
NC_000009.10:g.135122666A>T	NCBI36
NG_006669.1:g.20210T>A
NG_006669.2:g.22758T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.354T>A
ENST00000647353.1:n.54-6306T>A
ENST00000651471.1:n.329+584T>A
ENST00000679909.1:c.28+17704T>A	ENSP00000506089.1:n.28+17704T>A
ENST00000453660.3:n.336T>A
ENST00000538324.2:c.322T>A	ENSP00000483018.1:p.Phe108Ile
ENST00000611156.4:c.322T>A	ENSP00000483265.1:p.Phe108Ile
NM_020469.2:c.325T>A	NP_065202.2:p.Phe109Ile
NM_020469.3:c.325T>A	NP_065202.2:p.Phe109Ile