Canonical Allele Identifier: CA797777137
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1272449429
gnomAD v3: 4-68646618-TTTTTC-T
gnomAD v4: 4-68646618-TTTTTC-T
MyVariant Identifiers: chr4:g.69512337_69512341del (hg19) chr4:g.68646619_68646623del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646628_68646632del , CM000666.2:g.68646628_68646632del GRCh38
NC_000004.11:g.69512346_69512350del , CM000666.1:g.69512346_69512350del GRCh37
NC_000004.10:g.69194941_69194945del NCBI36
NG_052676.1:g.29154_29158del

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*481_*485del MANE Select ENSP00000341045.5:n.*481_*485del
ENST00000616841.4:c.1732+342_1732+346del ENSP00000482004.1:n.1732+342_1732+346del
NM_001076.3:c.*481_*485del NP_001067.2:n.*481_*485del
NM_001076.4:c.*481_*485del MANE Select NP_001067.2:n.*481_*485del
Search 100 bp 5'
Search 100 bp 3'