Canonical Allele Identifier: CA1882583318
Gene: ABO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133258255A= , CM000671.2:g.133258255A= GRCh38
NC_000009.11:g.136133646A= , CM000671.1:g.136133646A= GRCh37
NC_000009.10:g.135123467A= NCBI36
NG_006669.1:g.19408T=
NG_006669.2:g.21960T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.234-123T=
ENST00000647353.1:n.54-7103T=
ENST00000651471.1:n.239-123T=
ENST00000679909.1:c.28+16907T= ENSP00000506089.1:n.28+16907T=
ENST00000453660.3:n.216-123T=
ENST00000538324.2:c.204-123T= ENSP00000483018.1:n.204-123T=
ENST00000611156.4:c.204-123T= ENSP00000483265.1:n.204-123T=
NM_020469.2:c.204-123T= NP_065202.2:n.204-123T=
NM_020469.3:c.204-123T= NP_065202.2:n.204-123T=
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