Canonical Allele Identifier: CA1882585077
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133261756T= , CM000671.2:g.133261756T= GRCh38
NC_000009.11:g.136137159T= , CM000671.1:g.136137159T= GRCh37
NC_000009.10:g.135126980T= NCBI36
NG_006669.1:g.15894A=
NG_006669.2:g.18459A=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.128+343A=
ENST00000647353.1:n.54-10604A=
ENST00000651471.1:n.133+343A=
ENST00000679909.1:c.28+13406A= ENSP00000506089.1:n.28+13406A=
ENST00000453660.3:n.110+343A=
ENST00000538324.2:c.98+343A= ENSP00000483018.1:n.98+343A=
ENST00000611156.4:c.98+343A= ENSP00000483265.1:n.98+343A=
NM_020469.2:c.98+343A= NP_065202.2:n.98+343A=
NM_020469.3:c.98+343A= NP_065202.2:n.98+343A=