Canonical Allele Identifier: CA467783018

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131743T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256356T>C , CM000671.2:g.133256356T>C	GRCh38
NC_000009.11:g.136131743T>C , CM000671.1:g.136131743T>C	GRCh37
NC_000009.10:g.135121564T>C	NCBI36
NG_006669.1:g.21312A>G
NG_006669.2:g.23860A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.404A>G
ENST00000647353.1:n.54-5204A>G
ENST00000651471.1:n.330A>G
ENST00000679909.1:c.28+18806A>G	ENSP00000506089.1:n.28+18806A>G
ENST00000453660.3:n.386A>G
ENST00000538324.2:c.372A>G	ENSP00000483018.1:p.Lys124=
ENST00000611156.4:c.372A>G	ENSP00000483265.1:p.Lys124=
NM_020469.2:c.375A>G	NP_065202.2:p.Lys125=
NM_020469.3:c.375A>G	NP_065202.2:p.Lys125=