Canonical Allele Identifier: CA375686766

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136132909A>C (hg19) ; chr9:g.133257522A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133257522A>C , CM000671.2:g.133257522A>C	GRCh38
NC_000009.11:g.136132909A>C , CM000671.1:g.136132909A>C	GRCh37
NC_000009.10:g.135122730A>C	NCBI36
NG_006669.1:g.20145T>G
NG_006669.2:g.22693T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.290T>G
ENST00000647353.1:n.54-6370T>G
ENST00000651471.1:n.329+520T>G
ENST00000679909.1:c.28+17640T>G	ENSP00000506089.1:n.28+17640T>G
ENST00000453660.3:n.272T>G
ENST00000538324.2:c.259-1T>G	ENSP00000483018.1:n.259-1T>G
ENST00000611156.4:c.259-1T>G	ENSP00000483265.1:n.259-1T>G
NM_020469.2:c.260T>G	NP_065202.2:p.Val87Gly
NM_020469.3:c.260T>G	NP_065202.2:p.Val87Gly