Canonical Allele Identifier: CA2670844561
Gene: UGT2B15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670278_68670280del , CM000666.2:g.68670278_68670280del GRCh38
NC_000004.11:g.69535996_69535998del , CM000666.1:g.69535996_69535998del GRCh37
NC_000004.10:g.69218591_69218593del NCBI36
NG_052676.1:g.5498_5500del

Transcript Alleles

HGVS Amino-acid change
ENST00000338206.6:c.340_342del MANE Select ENSP00000341045.5:p.Gln114del
ENST00000338206.5:c.340_342del ENSP00000341045.5:p.Gln114del
ENST00000616841.4:c.340_342del ENSP00000482004.1:p.Gln114del
NM_001076.3:c.340_342del NP_001067.2:p.Gln114del
NM_001076.4:c.340_342del MANE Select NP_001067.2:p.Gln114del