Canonical Allele Identifier: CA1882578729
Gene: ABO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255450T= , CM000671.2:g.133255450T= GRCh38
NC_000009.11:g.136130837T= , CM000671.1:g.136130837T= GRCh37
NC_000009.10:g.135120658T= NCBI36
NG_006669.1:g.22218A=
NG_006669.2:g.24766A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1310A=
ENST00000647353.1:n.54-4298A=
ENST00000679909.1:c.28+19712A= ENSP00000506089.1:n.28+19712A=
ENST00000453660.3:n.1292A=
ENST00000611156.4:c.*216A= ENSP00000483265.1:n.*216A=
NM_020469.2:c.*216A= NP_065202.2:n.*216A=
NM_020469.3:c.*216A= NP_065202.2:n.*216A=
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