Canonical Allele Identifier: CA1465795117
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1733291358

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670753G>A , CM000666.2:g.68670753G>A GRCh38
NC_000004.11:g.69536471G>A , CM000666.1:g.69536471G>A GRCh37
NC_000004.10:g.69219066G>A NCBI36
NG_052676.1:g.5024C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-135C>T NP_001067.2:n.-135C>T