Canonical Allele Identifier: CA2670844559
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68670207-TAA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670208_68670209del , CM000666.2:g.68670208_68670209del GRCh38
NC_000004.11:g.69535926_69535927del , CM000666.1:g.69535926_69535927del GRCh37
NC_000004.10:g.69218521_69218522del NCBI36
NG_052676.1:g.5568_5569del

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.410_411del MANE Select ENSP00000341045.5:p.Leu137HisfsTer10
ENST00000338206.5:c.410_411del ENSP00000341045.5:p.Leu137HisfsTer10
ENST00000616841.4:c.410_411del ENSP00000482004.1:p.Leu137HisfsTer10
NM_001076.3:c.410_411del NP_001067.2:p.Leu137HisfsTer10
NM_001076.4:c.410_411del MANE Select NP_001067.2:p.Leu137HisfsTer10
Search 100 bp 5'
Search 100 bp 3'