Canonical Allele Identifier: CA1882580118
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256003G= , CM000671.2:g.133256003G= GRCh38
NC_000009.11:g.136131390G= , CM000671.1:g.136131390G= GRCh37
NC_000009.10:g.135121211G= NCBI36
NG_006669.1:g.21665C=
NG_006669.2:g.24213C=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.757C=
ENST00000647353.1:n.54-4851C=
ENST00000679909.1:c.28+19159C= ENSP00000506089.1:n.28+19159C=
ENST00000453660.3:n.739C=
ENST00000538324.2:c.725C= ENSP00000483018.1:p.Ala242=
ENST00000611156.4:c.725C= ENSP00000483265.1:p.Ala242=
NM_020469.2:c.728C= NP_065202.2:p.Ala243=
NM_020469.3:c.728C= NP_065202.2:p.Ala243=