Canonical Allele Identifier: CA1882579082
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255617G= , CM000671.2:g.133255617G= GRCh38
NC_000009.11:g.136131004G= , CM000671.1:g.136131004G= GRCh37
NC_000009.10:g.135120825G= NCBI36
NG_006669.1:g.22051C=
NG_006669.2:g.24599C=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.1143C=
ENST00000647353.1:n.54-4465C=
ENST00000679909.1:c.28+19545C= ENSP00000506089.1:n.28+19545C=
ENST00000453660.3:n.1125C=
ENST00000538324.2:c.1107C= ENSP00000483018.1:p.Ser369=
ENST00000611156.4:c.*49C= ENSP00000483265.1:n.*49C=
NM_020469.2:c.*49C= NP_065202.2:n.*49C=
NM_020469.3:c.*49C= NP_065202.2:n.*49C=