Canonical Allele Identifier: CA1882578389
Gene: ABO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255312C= , CM000671.2:g.133255312C= GRCh38
NC_000009.11:g.136130699C= , CM000671.1:g.136130699C= GRCh37
NC_000009.10:g.135120520C= NCBI36
NG_006669.1:g.22356G=
NG_006669.2:g.24904G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1448G=
ENST00000647353.1:n.54-4160G=
ENST00000679909.1:c.28+19850G= ENSP00000506089.1:n.28+19850G=
ENST00000453660.3:n.1430G=
ENST00000611156.4:c.*354G= ENSP00000483265.1:n.*354G=
NM_020469.2:c.*354G= NP_065202.2:n.*354G=
NM_020469.3:c.*354G= NP_065202.2:n.*354G=
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