Canonical Allele Identifier: CA1882584468
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133260366C= , CM000671.2:g.133260366C= GRCh38
NC_000009.11:g.136135769C= , CM000671.1:g.136135769C= GRCh37
NC_000009.10:g.135125590C= NCBI36
NG_006669.1:g.17284G=
NG_006669.2:g.19849G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.186-500G=
ENST00000647353.1:n.54-9214G=
ENST00000651471.1:n.191-500G=
ENST00000679909.1:c.28+14796G= ENSP00000506089.1:n.28+14796G=
ENST00000453660.3:n.168-500G=
ENST00000538324.2:c.156-500G= ENSP00000483018.1:n.156-500G=
ENST00000611156.4:c.156-500G= ENSP00000483265.1:n.156-500G=
NM_020469.2:c.156-500G= NP_065202.2:n.156-500G=
NM_020469.3:c.156-500G= NP_065202.2:n.156-500G=