Canonical Allele Identifier: CA375686587

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136132827T>A (hg19) ; chr9:g.133257440T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133257440T>A , CM000671.2:g.133257440T>A	GRCh38
NC_000009.11:g.136132827T>A , CM000671.1:g.136132827T>A	GRCh37
NC_000009.10:g.135122648T>A	NCBI36
NG_006669.1:g.20228A>T
NG_006669.2:g.22776A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.372A>T
ENST00000647353.1:n.54-6288A>T
ENST00000651471.1:n.329+602A>T
ENST00000679909.1:c.28+17722A>T	ENSP00000506089.1:n.28+17722A>T
ENST00000453660.3:n.354A>T
ENST00000538324.2:c.340A>T	ENSP00000483018.1:p.Thr114Ser
ENST00000611156.4:c.340A>T	ENSP00000483265.1:p.Thr114Ser
NM_020469.2:c.343A>T	NP_065202.2:p.Thr115Ser
NM_020469.3:c.343A>T	NP_065202.2:p.Thr115Ser