Canonical Allele Identifier: CA1063770363
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1733290449
gnomAD v3: 4-68670730-T-C
gnomAD v4: 4-68670730-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670730T>C , CM000666.2:g.68670730T>C GRCh38
NC_000004.11:g.69536448T>C , CM000666.1:g.69536448T>C GRCh37
NC_000004.10:g.69219043T>C NCBI36
NG_052676.1:g.5047A>G

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-112A>G NP_001067.2:n.-112A>G