Canonical Allele Identifier: CA1882580430
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256135C= , CM000671.2:g.133256135C= GRCh38
NC_000009.11:g.136131522C= , CM000671.1:g.136131522C= GRCh37
NC_000009.10:g.135121343C= NCBI36
NG_006669.1:g.21533G=
NG_006669.2:g.24081G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.625G=
ENST00000647353.1:n.54-4983G=
ENST00000651471.1:n.551G=
ENST00000679909.1:c.28+19027G= ENSP00000506089.1:n.28+19027G=
ENST00000453660.3:n.607G=
ENST00000538324.2:c.593G= ENSP00000483018.1:p.Arg198=
ENST00000611156.4:c.593G= ENSP00000483265.1:p.Arg198=
NM_020469.2:c.596G= NP_065202.2:p.Arg199=
NM_020469.3:c.596G= NP_065202.2:p.Arg199=