Canonical Allele Identifier: CA1882578709
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255442G= , CM000671.2:g.133255442G= GRCh38
NC_000009.11:g.136130829G= , CM000671.1:g.136130829G= GRCh37
NC_000009.10:g.135120650G= NCBI36
NG_006669.1:g.22226C=
NG_006669.2:g.24774C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1318C=
ENST00000647353.1:n.54-4290C=
ENST00000679909.1:c.28+19720C= ENSP00000506089.1:n.28+19720C=
ENST00000453660.3:n.1300C=
ENST00000611156.4:c.*224C= ENSP00000483265.1:n.*224C=
NM_020469.2:c.*224C= NP_065202.2:n.*224C=
NM_020469.3:c.*224C= NP_065202.2:n.*224C=