Canonical Allele Identifier: CA2942673
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs773037651

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670029_68670031del , CM000666.2:g.68670029_68670031del GRCh38
NC_000004.11:g.69535747_69535749del , CM000666.1:g.69535747_69535749del GRCh37
NC_000004.10:g.69218342_69218344del NCBI36
NG_052676.1:g.5750_5752del

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.592_594del MANE Select ENSP00000341045.5:p.Val198del
ENST00000338206.5:c.592_594del ENSP00000341045.5:p.Val198del
ENST00000616841.4:c.592_594del ENSP00000482004.1:p.Val198del
NM_001076.3:c.592_594del NP_001067.2:p.Val198del
NM_001076.4:c.592_594del MANE Select NP_001067.2:p.Val198del