Canonical Allele Identifier: CA1465795019
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1733288108

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670663G>T , CM000666.2:g.68670663G>T GRCh38
NC_000004.11:g.69536381G>T , CM000666.1:g.69536381G>T GRCh37
NC_000004.10:g.69218976G>T NCBI36
NG_052676.1:g.5114C>A

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-45C>A NP_001067.2:n.-45C>A