Canonical Allele Identifier: CA1882585093
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133261789T= , CM000671.2:g.133261789T= GRCh38
NC_000009.11:g.136137192T= , CM000671.1:g.136137192T= GRCh37
NC_000009.10:g.135127013T= NCBI36
NG_006669.1:g.15861A=
NG_006669.2:g.18426A=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.128+310A=
ENST00000647353.1:n.54-10637A=
ENST00000651471.1:n.133+310A=
ENST00000679909.1:c.28+13373A= ENSP00000506089.1:n.28+13373A=
ENST00000453660.3:n.110+310A=
ENST00000538324.2:c.98+310A= ENSP00000483018.1:n.98+310A=
ENST00000611156.4:c.98+310A= ENSP00000483265.1:n.98+310A=
NM_020469.2:c.98+310A= NP_065202.2:n.98+310A=
NM_020469.3:c.98+310A= NP_065202.2:n.98+310A=