Canonical Allele Identifier: CA1882578682
Gene: ABO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255428C= , CM000671.2:g.133255428C= GRCh38
NC_000009.11:g.136130815C= , CM000671.1:g.136130815C= GRCh37
NC_000009.10:g.135120636C= NCBI36
NG_006669.1:g.22240G=
NG_006669.2:g.24788G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1332G=
ENST00000647353.1:n.54-4276G=
ENST00000679909.1:c.28+19734G= ENSP00000506089.1:n.28+19734G=
ENST00000453660.3:n.1314G=
ENST00000611156.4:c.*238G= ENSP00000483265.1:n.*238G=
NM_020469.2:c.*238G= NP_065202.2:n.*238G=
NM_020469.3:c.*238G= NP_065202.2:n.*238G=
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