Canonical Allele Identifier: CA2670844619
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68670736-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670736C>G , CM000666.2:g.68670736C>G GRCh38
NC_000004.11:g.69536454C>G , CM000666.1:g.69536454C>G GRCh37
NC_000004.10:g.69219049C>G NCBI36
NG_052676.1:g.5041G>C

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-118G>C NP_001067.2:n.-118G>C