Canonical Allele Identifier: CA1465795075
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1733289764

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670706A>C , CM000666.2:g.68670706A>C GRCh38
NC_000004.11:g.69536424A>C , CM000666.1:g.69536424A>C GRCh37
NC_000004.10:g.69219019A>C NCBI36
NG_052676.1:g.5071T>G

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-88T>G NP_001067.2:n.-88T>G