Canonical Allele Identifier: CA1063770405
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1733290839
gnomAD v3: 4-68670742-A-G
gnomAD v4: 4-68670742-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670742A>G , CM000666.2:g.68670742A>G GRCh38
NC_000004.11:g.69536460A>G , CM000666.1:g.69536460A>G GRCh37
NC_000004.10:g.69219055A>G NCBI36
NG_052676.1:g.5035T>C

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-124T>C NP_001067.2:n.-124T>C