Canonical Allele Identifier: CA1465795072
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1733289708
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670705A>G , CM000666.2:g.68670705A>G GRCh38
NC_000004.11:g.69536423A>G , CM000666.1:g.69536423A>G GRCh37
NC_000004.10:g.69219018A>G NCBI36
NG_052676.1:g.5072T>C

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-87T>C NP_001067.2:n.-87T>C
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