Canonical Allele Identifier: CA375685965

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131507A>T (hg19) ; chr9:g.133256120A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256120A>T , CM000671.2:g.133256120A>T	GRCh38
NC_000009.11:g.136131507A>T , CM000671.1:g.136131507A>T	GRCh37
NC_000009.10:g.135121328A>T	NCBI36
NG_006669.1:g.21548T>A
NG_006669.2:g.24096T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.640T>A
ENST00000647353.1:n.54-4968T>A
ENST00000651471.1:n.566T>A
ENST00000679909.1:c.28+19042T>A	ENSP00000506089.1:n.28+19042T>A
ENST00000453660.3:n.622T>A
ENST00000538324.2:c.608T>A	ENSP00000483018.1:p.Val203Glu
ENST00000611156.4:c.608T>A	ENSP00000483265.1:p.Val203Glu
NM_020469.2:c.611T>A	NP_065202.2:p.Val204Glu
NM_020469.3:c.611T>A	NP_065202.2:p.Val204Glu