Canonical Allele Identifier: CA375686565

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136132815T>A (hg19) ; chr9:g.133257428T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133257428T>A , CM000671.2:g.133257428T>A	GRCh38
NC_000009.11:g.136132815T>A , CM000671.1:g.136132815T>A	GRCh37
NC_000009.10:g.135122636T>A	NCBI36
NG_006669.1:g.20240A>T
NG_006669.2:g.22788A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.384A>T
ENST00000647353.1:n.54-6276A>T
ENST00000651471.1:n.329+614A>T
ENST00000679909.1:c.28+17734A>T	ENSP00000506089.1:n.28+17734A>T
ENST00000453660.3:n.366A>T
ENST00000538324.2:c.352A>T	ENSP00000483018.1:p.Thr118Ser
ENST00000611156.4:c.352A>T	ENSP00000483265.1:p.Thr118Ser
NM_020469.2:c.355A>T	NP_065202.2:p.Thr119Ser
NM_020469.3:c.355A>T	NP_065202.2:p.Thr119Ser