Canonical Allele Identifier: CA552185674

Gene: UGT2B15

Linked Data

• dbSNP Id: rs1374532270
• gnomAD v2: 4-69536483-G-T
• gnomAD v3: 4-68670765-G-T
• gnomAD v4: 4-68670765-G-T
• MyVariant Identifiers: chr4:g.69536483G>T (hg19) ; chr4:g.68670765G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68670765G>T , CM000666.2:g.68670765G>T	GRCh38
NC_000004.11:g.69536483G>T , CM000666.1:g.69536483G>T	GRCh37
NC_000004.10:g.69219078G>T	NCBI36
NG_052676.1:g.5012C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001076.3:c.-147C>A	NP_001067.2:n.-147C>A