Canonical Allele Identifier: CA1882578591
Gene: ABO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255384G= , CM000671.2:g.133255384G= GRCh38
NC_000009.11:g.136130771G= , CM000671.1:g.136130771G= GRCh37
NC_000009.10:g.135120592G= NCBI36
NG_006669.1:g.22284C=
NG_006669.2:g.24832C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1376C=
ENST00000647353.1:n.54-4232C=
ENST00000679909.1:c.28+19778C= ENSP00000506089.1:n.28+19778C=
ENST00000453660.3:n.1358C=
ENST00000611156.4:c.*282C= ENSP00000483265.1:n.*282C=
NM_020469.2:c.*282C= NP_065202.2:n.*282C=
NM_020469.3:c.*282C= NP_065202.2:n.*282C=
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