Canonical Allele Identifier: CA375685126

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131327T>A (hg19) ; chr9:g.133255940T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255940T>A , CM000671.2:g.133255940T>A	GRCh38
NC_000009.11:g.136131327T>A , CM000671.1:g.136131327T>A	GRCh37
NC_000009.10:g.135121148T>A	NCBI36
NG_006669.1:g.21728A>T
NG_006669.2:g.24276A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.820A>T
ENST00000647353.1:n.54-4788A>T
ENST00000679909.1:c.28+19222A>T	ENSP00000506089.1:n.28+19222A>T
ENST00000453660.3:n.802A>T
ENST00000538324.2:c.788A>T	ENSP00000483018.1:p.Tyr263Phe
ENST00000611156.4:c.788A>T	ENSP00000483265.1:p.Tyr263Phe
NM_020469.2:c.791A>T	NP_065202.2:p.Tyr264Phe
NM_020469.3:c.791A>T	NP_065202.2:p.Tyr264Phe