Canonical Allele Identifier: CA98760885

Gene: UGT2B15

Linked Data

• dbSNP Id: rs912236946
• gnomAD v2: 4-69536428-A-C
• gnomAD v3: 4-68670710-A-C
• gnomAD v4: 4-68670710-A-C
• MyVariant Identifiers: chr4:g.69536428A>C (hg19) ; chr4:g.68670710A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68670710A>C , CM000666.2:g.68670710A>C	GRCh38
NC_000004.11:g.69536428A>C , CM000666.1:g.69536428A>C	GRCh37
NC_000004.10:g.69219023A>C	NCBI36
NG_052676.1:g.5067T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001076.3:c.-92T>G	NP_001067.2:n.-92T>G