Canonical Allele Identifier: CA797795611
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1328030406
gnomAD v4: 4-68670558-CAGAGCTAAAGT-C
MyVariant Identifiers: chr4:g.69536277_69536287del (hg19) chr4:g.68670559_68670569del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670560_68670570del , CM000666.2:g.68670560_68670570del GRCh38
NC_000004.11:g.69536278_69536288del , CM000666.1:g.69536278_69536288del GRCh37
NC_000004.10:g.69218873_69218883del NCBI36
NG_052676.1:g.5208_5218del

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.50_60del MANE Select ENSP00000341045.5:p.Tyr17TrpfsTer?
ENST00000338206.5:c.50_60del ENSP00000341045.5:p.Tyr17TrpfsTer?
ENST00000616841.4:c.50_60del ENSP00000482004.1:p.Tyr17TrpfsTer?
NM_001076.3:c.50_60del NP_001067.2:p.Tyr17TrpfsTer?
NM_001076.4:c.50_60del MANE Select NP_001067.2:p.Tyr17TrpfsTer?
Search 100 bp 5'
Search 100 bp 3'