Canonical Allele Identifier: CA1882585048
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133261682C= , CM000671.2:g.133261682C= GRCh38
NC_000009.11:g.136137085C= , CM000671.1:g.136137085C= GRCh37
NC_000009.10:g.135126906C= NCBI36
NG_006669.1:g.15968G=
NG_006669.2:g.18533G=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.129-308G=
ENST00000647353.1:n.54-10530G=
ENST00000651471.1:n.134-308G=
ENST00000679909.1:c.28+13480G= ENSP00000506089.1:n.28+13480G=
ENST00000453660.3:n.111-308G=
ENST00000538324.2:c.99-308G= ENSP00000483018.1:n.99-308G=
ENST00000611156.4:c.99-308G= ENSP00000483265.1:n.99-308G=
NM_020469.2:c.99-308G= NP_065202.2:n.99-308G=
NM_020469.3:c.99-308G= NP_065202.2:n.99-308G=