Canonical Allele Identifier: CA1465793545
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1733246918

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68669824_68669829del , CM000666.2:g.68669824_68669829del GRCh38
NC_000004.11:g.69535542_69535547del , CM000666.1:g.69535542_69535547del GRCh37
NC_000004.10:g.69218137_69218142del NCBI36
NG_052676.1:g.5954_5959del

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.724+72_724+77del MANE Select ENSP00000341045.5:n.724+72_724+77del
ENST00000338206.5:c.724+72_724+77del ENSP00000341045.5:n.724+72_724+77del
ENST00000616841.4:c.724+72_724+77del ENSP00000482004.1:n.724+72_724+77del
NM_001076.3:c.724+72_724+77del NP_001067.2:n.724+72_724+77del
NM_001076.4:c.724+72_724+77del MANE Select NP_001067.2:n.724+72_724+77del