Canonical Allele Identifier: CA1882580124
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256004C= , CM000671.2:g.133256004C= GRCh38
NC_000009.11:g.136131391C= , CM000671.1:g.136131391C= GRCh37
NC_000009.10:g.135121212C= NCBI36
NG_006669.1:g.21664G=
NG_006669.2:g.24212G=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.756G=
ENST00000647353.1:n.54-4852G=
ENST00000679909.1:c.28+19158G= ENSP00000506089.1:n.28+19158G=
ENST00000453660.3:n.738G=
ENST00000538324.2:c.724G= ENSP00000483018.1:p.Ala242=
ENST00000611156.4:c.724G= ENSP00000483265.1:p.Ala242=
NM_020469.2:c.727G= NP_065202.2:p.Ala243=
NM_020469.3:c.727G= NP_065202.2:p.Ala243=