Canonical Allele Identifier: CA2706232169
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1733289708

Genomic Alleles

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

Transcript Alleles

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