Canonical Allele Identifier: CA357086290
Gene: UGT2B15 HGNC NCBI

Linked Data

ClinVar Variation Id: 3186191
ClinVar RCV Id: RCV004479589
COSMIC: COSM5689242
MyVariant Identifiers: chr4:g.69536018A>C (hg19) chr4:g.68670300A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670300A>C , CM000666.2:g.68670300A>C GRCh38
NC_000004.11:g.69536018A>C , CM000666.1:g.69536018A>C GRCh37
NC_000004.10:g.69218613A>C NCBI36
NG_052676.1:g.5477T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.319T>G MANE Select ENSP00000341045.5:p.Trp107Gly
ENST00000338206.5:c.319T>G ENSP00000341045.5:p.Trp107Gly
ENST00000616841.4:c.319T>G ENSP00000482004.1:p.Trp107Gly
NM_001076.3:c.319T>G NP_001067.2:p.Trp107Gly
NM_001076.4:c.319T>G MANE Select NP_001067.2:p.Trp107Gly
Search 100 bp 5'
Search 100 bp 3'