Canonical Allele Identifier: CA98760846

Gene: UGT2B15

Linked Data

• dbSNP Id: rs924826521
• MyVariant Identifiers: chr4:g.69536376T>C (hg19) ; chr4:g.68670658T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68670658T>C , CM000666.2:g.68670658T>C	GRCh38
NC_000004.11:g.69536376T>C , CM000666.1:g.69536376T>C	GRCh37
NC_000004.10:g.69218971T>C	NCBI36
NG_052676.1:g.5119A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001076.3:c.-40A>G	NP_001067.2:n.-40A>G