Canonical Allele Identifier: CA1465820683
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1732475330
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646611del , CM000666.2:g.68646611del GRCh38
NC_000004.11:g.69512329del , CM000666.1:g.69512329del GRCh37
NC_000004.10:g.69194924del NCBI36
NG_052676.1:g.29166del

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*493del MANE Select ENSP00000341045.5:n.*493del
ENST00000616841.4:c.1732+354del ENSP00000482004.1:n.1732+354del
NM_001076.3:c.*493del NP_001067.2:n.*493del
NM_001076.4:c.*493del MANE Select NP_001067.2:n.*493del
Search 100 bp 5'
Search 100 bp 3'