Canonical Allele Identifier: CA2942647
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs764970781
ExAC: 4:69535603 CAT / C
gnomAD v2: 4-69535603-CAT-C
gnomAD v4: 4-68669885-CAT-C
MyVariant Identifiers: chr4:g.69535604_69535605del (hg19) chr4:g.68669886_68669887del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68669886_68669887del , CM000666.2:g.68669886_68669887del GRCh38
NC_000004.11:g.69535604_69535605del , CM000666.1:g.69535604_69535605del GRCh37
NC_000004.10:g.69218199_69218200del NCBI36
NG_052676.1:g.5890_5891del

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.724+8_724+9del MANE Select ENSP00000341045.5:n.724+8_724+9del
ENST00000338206.5:c.724+8_724+9del ENSP00000341045.5:n.724+8_724+9del
ENST00000616841.4:c.724+8_724+9del ENSP00000482004.1:n.724+8_724+9del
NM_001076.3:c.724+8_724+9del NP_001067.2:n.724+8_724+9del
NM_001076.4:c.724+8_724+9del MANE Select NP_001067.2:n.724+8_724+9del
Search 100 bp 5'
Search 100 bp 3'