Canonical Allele Identifier: CA2670844562
Gene: UGT2B15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670292del , CM000666.2:g.68670292del GRCh38
NC_000004.11:g.69536010del , CM000666.1:g.69536010del GRCh37
NC_000004.10:g.69218605del NCBI36
NG_052676.1:g.5489del

Transcript Alleles

HGVS Amino-acid change
ENST00000338206.6:c.331del MANE Select ENSP00000341045.5:p.Ser111HisfsTer23
ENST00000338206.5:c.331del ENSP00000341045.5:p.Ser111HisfsTer23
ENST00000616841.4:c.331del ENSP00000482004.1:p.Ser111HisfsTer23
NM_001076.3:c.331del NP_001067.2:p.Ser111HisfsTer23
NM_001076.4:c.331del MANE Select NP_001067.2:p.Ser111HisfsTer23