Canonical Allele Identifier: CA552612256
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1278611332
gnomAD v2: 4-69535956-GAGC-G
gnomAD v4: 4-68670238-GAGC-G
MyVariant Identifiers: chr4:g.69535957_69535959del (hg19) chr4:g.68670239_68670241del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670239_68670241del , CM000666.2:g.68670239_68670241del GRCh38
NC_000004.11:g.69535957_69535959del , CM000666.1:g.69535957_69535959del GRCh37
NC_000004.10:g.69218552_69218554del NCBI36
NG_052676.1:g.5536_5538del

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.378_380del MANE Select ENSP00000341045.5:p.Lys126_Leu127delinsAsn
ENST00000338206.5:c.378_380del ENSP00000341045.5:p.Lys126_Leu127delinsAsn
ENST00000616841.4:c.378_380del ENSP00000482004.1:p.Lys126_Leu127delinsAsn
NM_001076.3:c.378_380del NP_001067.2:p.Lys126_Leu127delinsAsn
NM_001076.4:c.378_380del MANE Select NP_001067.2:p.Lys126_Leu127delinsAsn
Search 100 bp 5'
Search 100 bp 3'