Canonical Allele Identifier: CA1882584461
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133260357G= , CM000671.2:g.133260357G= GRCh38
NC_000009.11:g.136135760G= , CM000671.1:g.136135760G= GRCh37
NC_000009.10:g.135125581G= NCBI36
NG_006669.1:g.17293C=
NG_006669.2:g.19858C=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.186-491C=
ENST00000647353.1:n.54-9205C=
ENST00000651471.1:n.191-491C=
ENST00000679909.1:c.28+14805C= ENSP00000506089.1:n.28+14805C=
ENST00000453660.3:n.168-491C=
ENST00000538324.2:c.156-491C= ENSP00000483018.1:n.156-491C=
ENST00000611156.4:c.156-491C= ENSP00000483265.1:n.156-491C=
NM_020469.2:c.156-491C= NP_065202.2:n.156-491C=
NM_020469.3:c.156-491C= NP_065202.2:n.156-491C=