Canonical Allele Identifier: CA1882584391
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133260148G= , CM000671.2:g.133260148G= GRCh38
NC_000009.11:g.136135552G= , CM000671.1:g.136135552G= GRCh37
NC_000009.10:g.135125373G= NCBI36
NG_006669.1:g.17502C=
NG_006669.2:g.20067C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.186-282C=
ENST00000647353.1:n.54-8996C=
ENST00000651471.1:n.191-282C=
ENST00000679909.1:c.28+15014C= ENSP00000506089.1:n.28+15014C=
ENST00000453660.3:n.168-282C=
ENST00000538324.2:c.156-282C= ENSP00000483018.1:n.156-282C=
ENST00000611156.4:c.156-282C= ENSP00000483265.1:n.156-282C=
NM_020469.2:c.156-282C= NP_065202.2:n.156-282C=
NM_020469.3:c.156-282C= NP_065202.2:n.156-282C=