Canonical Allele Identifier: CA2670843614
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68646922-CAT-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646924_68646925del , CM000666.2:g.68646924_68646925del GRCh38
NC_000004.11:g.69512642_69512643del , CM000666.1:g.69512642_69512643del GRCh37
NC_000004.10:g.69195237_69195238del NCBI36
NG_052676.1:g.28853_28854del

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*180_*181del MANE Select ENSP00000341045.5:n.*180_*181del
ENST00000338206.5:c.*180_*181del ENSP00000341045.5:n.*180_*181del
ENST00000616841.4:c.1732+41_1732+42del ENSP00000482004.1:n.1732+41_1732+42del
NM_001076.3:c.*180_*181del NP_001067.2:n.*180_*181del
NM_001076.4:c.*180_*181del MANE Select NP_001067.2:n.*180_*181del
Search 100 bp 5'
Search 100 bp 3'