Canonical Allele Identifier: CA1882582678
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257721C= , CM000671.2:g.133257721C= GRCh38
NC_000009.11:g.136133108C= , CM000671.1:g.136133108C= GRCh37
NC_000009.10:g.135122929C= NCBI36
NG_006669.1:g.19946G=
NG_006669.2:g.22494G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.270-179G=
ENST00000647353.1:n.54-6569G=
ENST00000651471.1:n.329+321G=
ENST00000679909.1:c.28+17441G= ENSP00000506089.1:n.28+17441G=
ENST00000453660.3:n.252-179G=
ENST00000538324.2:c.240-179G= ENSP00000483018.1:n.240-179G=
ENST00000611156.4:c.240-179G= ENSP00000483265.1:n.240-179G=
NM_020469.2:c.240-179G= NP_065202.2:n.240-179G=
NM_020469.3:c.240-179G= NP_065202.2:n.240-179G=