Canonical Allele Identifier: CA1465795115
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1733291218
gnomAD v4: 4-68670751-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670751C>T , CM000666.2:g.68670751C>T GRCh38
NC_000004.11:g.69536469C>T , CM000666.1:g.69536469C>T GRCh37
NC_000004.10:g.69219064C>T NCBI36
NG_052676.1:g.5026G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-133G>A NP_001067.2:n.-133G>A