Canonical Allele Identifier: CA357085576
Gene: UGT2B15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670178A>T , CM000666.2:g.68670178A>T GRCh38
NC_000004.11:g.69535896A>T , CM000666.1:g.69535896A>T GRCh37
NC_000004.10:g.69218491A>T NCBI36
NG_052676.1:g.5599T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000338206.6:c.441T>A MANE Select ENSP00000341045.5:p.Asp147Glu
ENST00000338206.5:c.441T>A ENSP00000341045.5:p.Asp147Glu
ENST00000616841.4:c.441T>A ENSP00000482004.1:p.Asp147Glu
NM_001076.3:c.441T>A NP_001067.2:p.Asp147Glu
NM_001076.4:c.441T>A MANE Select NP_001067.2:p.Asp147Glu