Canonical Allele Identifier: CA2942682
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs761679257
gnomAD v2: 4-69535792-T-C
gnomAD v4: 4-68670074-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670074T>C , CM000666.2:g.68670074T>C GRCh38
NC_000004.11:g.69535792T>C , CM000666.1:g.69535792T>C GRCh37
NC_000004.10:g.69218387T>C NCBI36
NG_052676.1:g.5703A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.545A>G MANE Select ENSP00000341045.5:p.Glu182Gly
ENST00000338206.5:c.545A>G ENSP00000341045.5:p.Glu182Gly
ENST00000616841.4:c.545A>G ENSP00000482004.1:p.Glu182Gly
NM_001076.3:c.545A>G NP_001067.2:p.Glu182Gly
NM_001076.4:c.545A>G MANE Select NP_001067.2:p.Glu182Gly