Canonical Allele Identifier: CA552185665

Gene: UGT2B15

Linked Data

• dbSNP Id: rs781485665
• gnomAD v2: 4-69536359-T-G
• gnomAD v4: 4-68670641-T-G
• MyVariant Identifiers: chr4:g.69536359T>G (hg19) ; chr4:g.68670641T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68670641T>G , CM000666.2:g.68670641T>G	GRCh38
NC_000004.11:g.69536359T>G , CM000666.1:g.69536359T>G	GRCh37
NC_000004.10:g.69218954T>G	NCBI36
NG_052676.1:g.5136A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.-23A>C MANE Select	ENSP00000341045.5:n.-23A>C
NM_001076.3:c.-23A>C	NP_001067.2:n.-23A>C
NM_001076.4:c.-23A>C MANE Select	NP_001067.2:n.-23A>C