Canonical Allele Identifier: CA797795835

Gene: UGT2B15

Linked Data

• dbSNP Id: rs1344353369
• gnomAD v3: 4-68670755-A-AT
• gnomAD v4: 4-68670755-A-AT
• MyVariant Identifiers: chr4:g.69536473_69536474insT (hg19) ; chr4:g.68670755_68670756insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68670756dup , CM000666.2:g.68670756dup	GRCh38
NC_000004.11:g.69536474dup , CM000666.1:g.69536474dup	GRCh37
NC_000004.10:g.69219069dup	NCBI36
NG_052676.1:g.5021dup

Transcript Alleles

HGVS	Amino-acid Change
NM_001076.3:c.-138dup	NP_001067.2:n.-138dup