Canonical Allele Identifier: CA1882579685
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255852G= , CM000671.2:g.133255852G= GRCh38
NC_000009.11:g.136131239G= , CM000671.1:g.136131239G= GRCh37
NC_000009.10:g.135121060G= NCBI36
NG_006669.1:g.21816C=
NG_006669.2:g.24364C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.908C=
ENST00000647353.1:n.54-4700C=
ENST00000679909.1:c.28+19310C= ENSP00000506089.1:n.28+19310C=
ENST00000453660.3:n.890C=
ENST00000538324.2:c.876C= ENSP00000483018.1:p.Ala292=
ENST00000611156.4:c.876C= ENSP00000483265.1:p.Ala292=
NM_020469.2:c.879C= NP_065202.2:p.Ala293=
NM_020469.3:c.879C= NP_065202.2:p.Ala293=