Canonical Allele Identifier: CA1063770342
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1733289404
gnomAD v3: 4-68670695-C-A
gnomAD v4: 4-68670695-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670695C>A , CM000666.2:g.68670695C>A GRCh38
NC_000004.11:g.69536413C>A , CM000666.1:g.69536413C>A GRCh37
NC_000004.10:g.69219008C>A NCBI36
NG_052676.1:g.5082G>T

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-77G>T NP_001067.2:n.-77G>T