Canonical Allele Identifier: CA5305805
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs781828747

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256170G>A , CM000671.2:g.133256170G>A GRCh38
NC_000009.11:g.136131557G>A , CM000671.1:g.136131557G>A GRCh37
NC_000009.10:g.135121378G>A NCBI36
NG_006669.1:g.21498C>T
NG_006669.2:g.24046C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.590C>T
ENST00000647353.1:n.54-5018C>T
ENST00000651471.1:n.516C>T
ENST00000679909.1:c.28+18992C>T ENSP00000506089.1:n.28+18992C>T
ENST00000453660.3:n.572C>T
ENST00000538324.2:c.558C>T ENSP00000483018.1:p.Arg186=
ENST00000611156.4:c.558C>T ENSP00000483265.1:p.Arg186=
NM_020469.2:c.561C>T NP_065202.2:p.Arg187=
NM_020469.3:c.561C>T NP_065202.2:p.Arg187=