Canonical Allele Identifier: CA1882579798
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255902C= , CM000671.2:g.133255902C= GRCh38
NC_000009.11:g.136131289C= , CM000671.1:g.136131289C= GRCh37
NC_000009.10:g.135121110C= NCBI36
NG_006669.1:g.21766G=
NG_006669.2:g.24314G=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.858G=
ENST00000647353.1:n.54-4750G=
ENST00000679909.1:c.28+19260G= ENSP00000506089.1:n.28+19260G=
ENST00000453660.3:n.840G=
ENST00000538324.2:c.826G= ENSP00000483018.1:p.Val276=
ENST00000611156.4:c.826G= ENSP00000483265.1:p.Val276=
NM_020469.2:c.829G= NP_065202.2:p.Val277=
NM_020469.3:c.829G= NP_065202.2:p.Val277=