Canonical Allele Identifier: CA2670843635
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68646934-CAG-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646935_68646936del , CM000666.2:g.68646935_68646936del GRCh38
NC_000004.11:g.69512653_69512654del , CM000666.1:g.69512653_69512654del GRCh37
NC_000004.10:g.69195248_69195249del NCBI36
NG_052676.1:g.28841_28842del

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*168_*169del MANE Select ENSP00000341045.5:n.*168_*169del
ENST00000338206.5:c.*168_*169del ENSP00000341045.5:n.*168_*169del
ENST00000616841.4:c.1732+29_1732+30del ENSP00000482004.1:n.1732+29_1732+30del
NM_001076.3:c.*168_*169del NP_001067.2:n.*168_*169del
NM_001076.4:c.*168_*169del MANE Select NP_001067.2:n.*168_*169del
Search 100 bp 5'
Search 100 bp 3'