Canonical Allele Identifier: CA467783578
Gene: ABO HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.136132825G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257438G>A , CM000671.2:g.133257438G>A GRCh38
NC_000009.11:g.136132825G>A , CM000671.1:g.136132825G>A GRCh37
NC_000009.10:g.135122646G>A NCBI36
NG_006669.1:g.20230C>T
NG_006669.2:g.22778C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.374C>T
ENST00000647353.1:n.54-6286C>T
ENST00000651471.1:n.329+604C>T
ENST00000679909.1:c.28+17724C>T ENSP00000506089.1:n.28+17724C>T
ENST00000453660.3:n.356C>T
ENST00000538324.2:c.342C>T ENSP00000483018.1:p.Thr114=
ENST00000611156.4:c.342C>T ENSP00000483265.1:p.Thr114=
NM_020469.2:c.345C>T NP_065202.2:p.Thr115=
NM_020469.3:c.345C>T NP_065202.2:p.Thr115=