Canonical Allele Identifier: CA552612254
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1359605373
gnomAD v2: 4-69535850-CAGCCAGT-C
gnomAD v3: 4-68670132-CAGCCAGT-C
gnomAD v4: 4-68670132-CAGCCAGT-C
MyVariant Identifiers: chr4:g.69535851_69535857del (hg19) chr4:g.68670133_68670139del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670136_68670142del , CM000666.2:g.68670136_68670142del GRCh38
NC_000004.11:g.69535854_69535860del , CM000666.1:g.69535854_69535860del GRCh37
NC_000004.10:g.69218449_69218455del NCBI36
NG_052676.1:g.5638_5644del

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.480_486del MANE Select ENSP00000341045.5:p.Leu161AsnfsTer?
ENST00000338206.5:c.480_486del ENSP00000341045.5:p.Leu161AsnfsTer?
ENST00000616841.4:c.480_486del ENSP00000482004.1:p.Leu161AsnfsTer?
NM_001076.3:c.480_486del NP_001067.2:p.Leu161AsnfsTer?
NM_001076.4:c.480_486del MANE Select NP_001067.2:p.Leu161AsnfsTer?
Search 100 bp 5'
Search 100 bp 3'