Canonical Allele Identifier: CA375686700

Gene: ABO

Linked Data

• dbSNP Id: rs2118948065
• MyVariant Identifiers: chr9:g.136132878C>T (hg19) ; chr9:g.133257491C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133257491C>T , CM000671.2:g.133257491C>T	GRCh38
NC_000009.11:g.136132878C>T , CM000671.1:g.136132878C>T	GRCh37
NC_000009.10:g.135122699C>T	NCBI36
NG_006669.1:g.20177G>A
NG_006669.2:g.22725G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.321G>A
ENST00000647353.1:n.54-6339G>A
ENST00000651471.1:n.329+551G>A
ENST00000679909.1:c.28+17671G>A	ENSP00000506089.1:n.28+17671G>A
ENST00000453660.3:n.303G>A
ENST00000538324.2:c.289G>A	ENSP00000483018.1:p.Gly97Ser
ENST00000611156.4:c.289G>A	ENSP00000483265.1:p.Gly97Ser
NM_020469.2:c.292G>A	NP_065202.2:p.Gly98Ser
NM_020469.3:c.292G>A	NP_065202.2:p.Gly98Ser