Canonical Allele Identifier: CA1882584473
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133260377C= , CM000671.2:g.133260377C= GRCh38
NC_000009.11:g.136135780C= , CM000671.1:g.136135780C= GRCh37
NC_000009.10:g.135125601C= NCBI36
NG_006669.1:g.17273G=
NG_006669.2:g.19838G=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.186-511G=
ENST00000647353.1:n.54-9225G=
ENST00000651471.1:n.191-511G=
ENST00000679909.1:c.28+14785G= ENSP00000506089.1:n.28+14785G=
ENST00000453660.3:n.168-511G=
ENST00000538324.2:c.156-511G= ENSP00000483018.1:n.156-511G=
ENST00000611156.4:c.156-511G= ENSP00000483265.1:n.156-511G=
NM_020469.2:c.156-511G= NP_065202.2:n.156-511G=
NM_020469.3:c.156-511G= NP_065202.2:n.156-511G=