Canonical Allele Identifier: CA2670844638

Gene: UGT2B15

Linked Data

• gnomAD v4: 4-68670766-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68670766C>T , CM000666.2:g.68670766C>T	GRCh38
NC_000004.11:g.69536484C>T , CM000666.1:g.69536484C>T	GRCh37
NC_000004.10:g.69219079C>T	NCBI36
NG_052676.1:g.5011G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001076.3:c.-148G>A	NP_001067.2:n.-148G>A