Canonical Allele Identifier: CA375685307

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131384G>A (hg19) ; chr9:g.133255997G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255997G>A , CM000671.2:g.133255997G>A	GRCh38
NC_000009.11:g.136131384G>A , CM000671.1:g.136131384G>A	GRCh37
NC_000009.10:g.135121205G>A	NCBI36
NG_006669.1:g.21671C>T
NG_006669.2:g.24219C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.763C>T
ENST00000647353.1:n.54-4845C>T
ENST00000679909.1:c.28+19165C>T	ENSP00000506089.1:n.28+19165C>T
ENST00000453660.3:n.745C>T
ENST00000538324.2:c.731C>T	ENSP00000483018.1:p.Thr244Ile
ENST00000611156.4:c.731C>T	ENSP00000483265.1:p.Thr244Ile
NM_020469.2:c.734C>T	NP_065202.2:p.Thr245Ile
NM_020469.3:c.734C>T	NP_065202.2:p.Thr245Ile