Canonical Allele Identifier: CA552185673

Gene: UGT2B15

Linked Data

• dbSNP Id: rs1202161290
• gnomAD v2: 4-69536436-T-A
• gnomAD v3: 4-68670718-T-A
• gnomAD v4: 4-68670718-T-A
• MyVariant Identifiers: chr4:g.69536436T>A (hg19) ; chr4:g.68670718T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68670718T>A , CM000666.2:g.68670718T>A	GRCh38
NC_000004.11:g.69536436T>A , CM000666.1:g.69536436T>A	GRCh37
NC_000004.10:g.69219031T>A	NCBI36
NG_052676.1:g.5059A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001076.3:c.-100A>T	NP_001067.2:n.-100A>T