Canonical Allele Identifier: CA357085249
Gene: UGT2B15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670075C>T , CM000666.2:g.68670075C>T GRCh38
NC_000004.11:g.69535793C>T , CM000666.1:g.69535793C>T GRCh37
NC_000004.10:g.69218388C>T NCBI36
NG_052676.1:g.5702G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.544G>A MANE Select ENSP00000341045.5:p.Glu182Lys
ENST00000338206.5:c.544G>A ENSP00000341045.5:p.Glu182Lys
ENST00000616841.4:c.544G>A ENSP00000482004.1:p.Glu182Lys
NM_001076.3:c.544G>A NP_001067.2:p.Glu182Lys
NM_001076.4:c.544G>A MANE Select NP_001067.2:p.Glu182Lys