Canonical Allele Identifier: CA98759660
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1021983890
gnomAD v2: 4-69535525-ATC-A
gnomAD v3: 4-68669807-ATC-A
gnomAD v4: 4-68669807-ATC-A
MyVariant Identifiers: chr4:g.69535526_69535527del (hg19) chr4:g.68669808_68669809del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68669809_68669810del , CM000666.2:g.68669809_68669810del GRCh38
NC_000004.11:g.69535527_69535528del , CM000666.1:g.69535527_69535528del GRCh37
NC_000004.10:g.69218122_69218123del NCBI36
NG_052676.1:g.5968_5969del

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.724+86_724+87del MANE Select ENSP00000341045.5:n.724+86_724+87del
ENST00000338206.5:c.724+86_724+87del ENSP00000341045.5:n.724+86_724+87del
ENST00000616841.4:c.724+86_724+87del ENSP00000482004.1:n.724+86_724+87del
NM_001076.3:c.724+86_724+87del NP_001067.2:n.724+86_724+87del
NM_001076.4:c.724+86_724+87del MANE Select NP_001067.2:n.724+86_724+87del
Search 100 bp 5'
Search 100 bp 3'