Canonical Allele Identifier: CA1882580836
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256268G= , CM000671.2:g.133256268G= GRCh38
NC_000009.11:g.136131655G= , CM000671.1:g.136131655G= GRCh37
NC_000009.10:g.135121476G= NCBI36
NG_006669.1:g.21400C=
NG_006669.2:g.23948C=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.492C=
ENST00000647353.1:n.54-5116C=
ENST00000651471.1:n.418C=
ENST00000679909.1:c.28+18894C= ENSP00000506089.1:n.28+18894C=
ENST00000453660.3:n.474C=
ENST00000538324.2:c.460C= ENSP00000483018.1:p.Gln154=
ENST00000611156.4:c.460C= ENSP00000483265.1:p.Gln154=
NM_020469.2:c.463C= NP_065202.2:p.Gln155=
NM_020469.3:c.463C= NP_065202.2:p.Gln155=