Canonical Allele Identifier: CA5305752
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs35494115

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256002G>A , CM000671.2:g.133256002G>A GRCh38
NC_000009.11:g.136131389G>A , CM000671.1:g.136131389G>A GRCh37
NC_000009.10:g.135121210G>A NCBI36
NG_006669.1:g.21666C>T
NG_006669.2:g.24214C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.758C>T
ENST00000647353.1:n.54-4850C>T
ENST00000679909.1:c.28+19160C>T ENSP00000506089.1:n.28+19160C>T
ENST00000453660.3:n.740C>T
ENST00000538324.2:c.726C>T ENSP00000483018.1:p.Ala242=
ENST00000611156.4:c.726C>T ENSP00000483265.1:p.Ala242=
NM_020469.2:c.729C>T NP_065202.2:p.Ala243=
NM_020469.3:c.729C>T NP_065202.2:p.Ala243=