Canonical Allele Identifier: CA552185670

Gene: UGT2B15

Linked Data

• dbSNP Id: rs1343900954
• gnomAD v2: 4-69536416-T-C
• gnomAD v3: 4-68670698-T-C
• gnomAD v4: 4-68670698-T-C
• MyVariant Identifiers: chr4:g.69536416T>C (hg19) ; chr4:g.68670698T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68670698T>C , CM000666.2:g.68670698T>C	GRCh38
NC_000004.11:g.69536416T>C , CM000666.1:g.69536416T>C	GRCh37
NC_000004.10:g.69219011T>C	NCBI36
NG_052676.1:g.5079A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001076.3:c.-80A>G	NP_001067.2:n.-80A>G