Canonical Allele Identifier: CA375686548

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136132806C>T (hg19) ; chr9:g.133257419C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133257419C>T , CM000671.2:g.133257419C>T	GRCh38
NC_000009.11:g.136132806C>T , CM000671.1:g.136132806C>T	GRCh37
NC_000009.10:g.135122627C>T	NCBI36
NG_006669.1:g.20249G>A
NG_006669.2:g.22797G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.393G>A
ENST00000647353.1:n.54-6267G>A
ENST00000651471.1:n.329+623G>A
ENST00000679909.1:c.28+17743G>A	ENSP00000506089.1:n.28+17743G>A
ENST00000453660.3:n.375G>A
ENST00000538324.2:c.361G>A	ENSP00000483018.1:p.Ala121Thr
ENST00000611156.4:c.361G>A	ENSP00000483265.1:p.Ala121Thr
NM_020469.2:c.364G>A	NP_065202.2:p.Ala122Thr
NM_020469.3:c.364G>A	NP_065202.2:p.Ala122Thr