Canonical Allele Identifier: CA98760884

Gene: UGT2B15

Linked Data

• dbSNP Id: rs1051161087
• gnomAD v2: 4-69536404-A-G
• gnomAD v3: 4-68670686-A-G
• gnomAD v4: 4-68670686-A-G
• MyVariant Identifiers: chr4:g.69536404A>G (hg19) ; chr4:g.68670686A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68670686A>G , CM000666.2:g.68670686A>G	GRCh38
NC_000004.11:g.69536404A>G , CM000666.1:g.69536404A>G	GRCh37
NC_000004.10:g.69218999A>G	NCBI36
NG_052676.1:g.5091T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001076.3:c.-68T>C	NP_001067.2:n.-68T>C