Canonical Allele Identifier: CA1882578669
Gene: ABO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255414T= , CM000671.2:g.133255414T= GRCh38
NC_000009.11:g.136130801T= , CM000671.1:g.136130801T= GRCh37
NC_000009.10:g.135120622T= NCBI36
NG_006669.1:g.22254A=
NG_006669.2:g.24802A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1346A=
ENST00000647353.1:n.54-4262A=
ENST00000679909.1:c.28+19748A= ENSP00000506089.1:n.28+19748A=
ENST00000453660.3:n.1328A=
ENST00000611156.4:c.*252A= ENSP00000483265.1:n.*252A=
NM_020469.2:c.*252A= NP_065202.2:n.*252A=
NM_020469.3:c.*252A= NP_065202.2:n.*252A=
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