Canonical Allele Identifier: CA5305707
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs782297129

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255888G>A , CM000671.2:g.133255888G>A GRCh38
NC_000009.11:g.136131275G>A , CM000671.1:g.136131275G>A GRCh37
NC_000009.10:g.135121096G>A NCBI36
NG_006669.1:g.21780C>T
NG_006669.2:g.24328C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.872C>T
ENST00000647353.1:n.54-4736C>T
ENST00000679909.1:c.28+19274C>T ENSP00000506089.1:n.28+19274C>T
ENST00000453660.3:n.854C>T
ENST00000538324.2:c.840C>T ENSP00000483018.1:p.Thr280=
ENST00000611156.4:c.840C>T ENSP00000483265.1:p.Thr280=
NM_020469.2:c.843C>T NP_065202.2:p.Thr281=
NM_020469.3:c.843C>T NP_065202.2:p.Thr281=