Canonical Allele Identifier: CA467853098

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131305C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255918C>A , CM000671.2:g.133255918C>A	GRCh38
NC_000009.11:g.136131305C>A , CM000671.1:g.136131305C>A	GRCh37
NC_000009.10:g.135121126C>A	NCBI36
NG_006669.1:g.21750G>T
NG_006669.2:g.24298G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.842G>T
ENST00000647353.1:n.54-4766G>T
ENST00000679909.1:c.28+19244G>T	ENSP00000506089.1:n.28+19244G>T
ENST00000453660.3:n.824G>T
ENST00000538324.2:c.810G>T	ENSP00000483018.1:p.Gly270=
ENST00000611156.4:c.810G>T	ENSP00000483265.1:p.Gly270=
NM_020469.2:c.813G>T	NP_065202.2:p.Gly271=
NM_020469.3:c.813G>T	NP_065202.2:p.Gly271=