Canonical Allele Identifier: CA467852998
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1227462738

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256083G>A , CM000671.2:g.133256083G>A GRCh38
NC_000009.11:g.136131470G>A , CM000671.1:g.136131470G>A GRCh37
NC_000009.10:g.135121291G>A NCBI36
NG_006669.1:g.21585C>T
NG_006669.2:g.24133C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.677C>T
ENST00000647353.1:n.54-4931C>T
ENST00000679909.1:c.28+19079C>T ENSP00000506089.1:n.28+19079C>T
ENST00000453660.3:n.659C>T
ENST00000538324.2:c.645C>T ENSP00000483018.1:p.Phe215=
ENST00000611156.4:c.645C>T ENSP00000483265.1:p.Phe215=
NM_020469.2:c.648C>T NP_065202.2:p.Phe216=
NM_020469.3:c.648C>T NP_065202.2:p.Phe216=