Canonical Allele Identifier: CA1882578354
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255299C= , CM000671.2:g.133255299C= GRCh38
NC_000009.11:g.136130686C= , CM000671.1:g.136130686C= GRCh37
NC_000009.10:g.135120507C= NCBI36
NG_006669.1:g.22369G=
NG_006669.2:g.24917G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1461G=
ENST00000647353.1:n.54-4147G=
ENST00000679909.1:c.28+19863G= ENSP00000506089.1:n.28+19863G=
ENST00000453660.3:n.1443G=
ENST00000611156.4:c.*367G= ENSP00000483265.1:n.*367G=
NM_020469.2:c.*367G= NP_065202.2:n.*367G=
NM_020469.3:c.*367G= NP_065202.2:n.*367G=