Canonical Allele Identifier: CA1465795121
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1733291666
gnomAD v4: 4-68670758-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670758G>A , CM000666.2:g.68670758G>A GRCh38
NC_000004.11:g.69536476G>A , CM000666.1:g.69536476G>A GRCh37
NC_000004.10:g.69219071G>A NCBI36
NG_052676.1:g.5019C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-140C>T NP_001067.2:n.-140C>T