Canonical Allele Identifier: CA1882584382
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133260132C= , CM000671.2:g.133260132C= GRCh38
NC_000009.11:g.136135536C= , CM000671.1:g.136135536C= GRCh37
NC_000009.10:g.135125357C= NCBI36
NG_006669.1:g.17518G=
NG_006669.2:g.20083G=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.186-266G=
ENST00000647353.1:n.54-8980G=
ENST00000651471.1:n.191-266G=
ENST00000679909.1:c.28+15030G= ENSP00000506089.1:n.28+15030G=
ENST00000453660.3:n.168-266G=
ENST00000538324.2:c.156-266G= ENSP00000483018.1:n.156-266G=
ENST00000611156.4:c.156-266G= ENSP00000483265.1:n.156-266G=
NM_020469.2:c.156-266G= NP_065202.2:n.156-266G=
NM_020469.3:c.156-266G= NP_065202.2:n.156-266G=