Canonical Allele Identifier: CA357083016
Gene: UGT2B15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68647162A>T , CM000666.2:g.68647162A>T GRCh38
NC_000004.11:g.69512880A>T , CM000666.1:g.69512880A>T GRCh37
NC_000004.10:g.69195475A>T NCBI36
NG_052676.1:g.28615T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.1535T>A MANE Select ENSP00000341045.5:p.Phe512Tyr
ENST00000338206.5:c.1535T>A ENSP00000341045.5:p.Phe512Tyr
ENST00000616841.4:c.1535T>A ENSP00000482004.1:p.Phe512Tyr
NM_001076.3:c.1535T>A NP_001067.2:p.Phe512Tyr
NM_001076.4:c.1535T>A MANE Select NP_001067.2:p.Phe512Tyr