Canonical Allele Identifier: CA1882580275
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256067C= , CM000671.2:g.133256067C= GRCh38
NC_000009.11:g.136131454C= , CM000671.1:g.136131454C= GRCh37
NC_000009.10:g.135121275C= NCBI36
NG_006669.1:g.21601G=
NG_006669.2:g.24149G=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.693G=
ENST00000647353.1:n.54-4915G=
ENST00000679909.1:c.28+19095G= ENSP00000506089.1:n.28+19095G=
ENST00000453660.3:n.675G=
ENST00000538324.2:c.661G= ENSP00000483018.1:p.Val221=
ENST00000611156.4:c.661G= ENSP00000483265.1:p.Val221=
NM_020469.2:c.664G= NP_065202.2:p.Val222=
NM_020469.3:c.664G= NP_065202.2:p.Val222=