Canonical Allele Identifier: CA357086771
Gene: UGT2B15 HGNC NCBI

Linked Data

COSMIC: COSM402464

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670380G>C , CM000666.2:g.68670380G>C GRCh38
NC_000004.11:g.69536098G>C , CM000666.1:g.69536098G>C GRCh37
NC_000004.10:g.69218693G>C NCBI36
NG_052676.1:g.5397C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000338206.6:c.239C>G MANE Select ENSP00000341045.5:p.Ser80Cys
ENST00000338206.5:c.239C>G ENSP00000341045.5:p.Ser80Cys
ENST00000616841.4:c.239C>G ENSP00000482004.1:p.Ser80Cys
NM_001076.3:c.239C>G NP_001067.2:p.Ser80Cys
NM_001076.4:c.239C>G MANE Select NP_001067.2:p.Ser80Cys