Canonical Allele Identifier: CA1882580546
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256172G= , CM000671.2:g.133256172G= GRCh38
NC_000009.11:g.136131559G= , CM000671.1:g.136131559G= GRCh37
NC_000009.10:g.135121380G= NCBI36
NG_006669.1:g.21496C=
NG_006669.2:g.24044C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.588C=
ENST00000647353.1:n.54-5020C=
ENST00000651471.1:n.514C=
ENST00000679909.1:c.28+18990C= ENSP00000506089.1:n.28+18990C=
ENST00000453660.3:n.570C=
ENST00000538324.2:c.556C= ENSP00000483018.1:p.Arg186=
ENST00000611156.4:c.556C= ENSP00000483265.1:p.Arg186=
NM_020469.2:c.559C= NP_065202.2:p.Arg187=
NM_020469.3:c.559C= NP_065202.2:p.Arg187=