Canonical Allele Identifier: CA2942802
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs753983686
ExAC: 4:69536352 TG / T
gnomAD v2: 4-69536352-TG-T
gnomAD v3: 4-68670634-TG-T
gnomAD v4: 4-68670634-TG-T
MyVariant Identifiers: chr4:g.69536353del (hg19) chr4:g.68670635del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670635del , CM000666.2:g.68670635del GRCh38
NC_000004.11:g.69536353del , CM000666.1:g.69536353del GRCh37
NC_000004.10:g.69218948del NCBI36
NG_052676.1:g.5142del

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.-17del MANE Select ENSP00000341045.5:n.-17del
NM_001076.3:c.-17del NP_001067.2:n.-17del
NM_001076.4:c.-17del MANE Select NP_001067.2:n.-17del
Search 100 bp 5'
Search 100 bp 3'