Canonical Allele Identifier: CA1063770398
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1733290614
gnomAD v3: 4-68670735-A-T
gnomAD v4: 4-68670735-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670735A>T , CM000666.2:g.68670735A>T GRCh38
NC_000004.11:g.69536453A>T , CM000666.1:g.69536453A>T GRCh37
NC_000004.10:g.69219048A>T NCBI36
NG_052676.1:g.5042T>A

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-117T>A NP_001067.2:n.-117T>A