Canonical Allele Identifier: CA2670844611

Gene: UGT2B15

Linked Data

• gnomAD v4: 4-68670717-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68670717C>G , CM000666.2:g.68670717C>G	GRCh38
NC_000004.11:g.69536435C>G , CM000666.1:g.69536435C>G	GRCh37
NC_000004.10:g.69219030C>G	NCBI36
NG_052676.1:g.5060G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001076.3:c.-99G>C	NP_001067.2:n.-99G>C