Canonical Allele Identifier: CA1465794287
Gene: UGT2B15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670266C= , CM000666.2:g.68670266C= GRCh38
NC_000004.11:g.69535984C= , CM000666.1:g.69535984C= GRCh37
NC_000004.10:g.69218579C= NCBI36
NG_052676.1:g.5511G=

Transcript Alleles

HGVS Amino-acid change
ENST00000338206.6:c.353G= MANE Select ENSP00000341045.5:p.Trp118=
ENST00000338206.5:c.353G= ENSP00000341045.5:p.Trp118=
ENST00000616841.4:c.353G= ENSP00000482004.1:p.Trp118=
NM_001076.3:c.353G= NP_001067.2:p.Trp118=
NM_001076.4:c.353G= MANE Select NP_001067.2:p.Trp118=