Canonical Allele Identifier: CA1882579997
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255957C= , CM000671.2:g.133255957C= GRCh38
NC_000009.11:g.136131344C= , CM000671.1:g.136131344C= GRCh37
NC_000009.10:g.135121165C= NCBI36
NG_006669.1:g.21711G=
NG_006669.2:g.24259G=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.803G=
ENST00000647353.1:n.54-4805G=
ENST00000679909.1:c.28+19205G= ENSP00000506089.1:n.28+19205G=
ENST00000453660.3:n.785G=
ENST00000538324.2:c.771G= ENSP00000483018.1:p.Lys257=
ENST00000611156.4:c.771G= ENSP00000483265.1:p.Lys257=
NM_020469.2:c.774G= NP_065202.2:p.Lys258=
NM_020469.3:c.774G= NP_065202.2:p.Lys258=