Canonical Allele Identifier: CA1465794366
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1233102889
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670312_68670313del , CM000666.2:g.68670312_68670313del GRCh38
NC_000004.11:g.69536030_69536031del , CM000666.1:g.69536030_69536031del GRCh37
NC_000004.10:g.69218625_69218626del NCBI36
NG_052676.1:g.5468_5469del

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.310_311del MANE Select ENSP00000341045.5:p.Asn104TyrfsTer18
ENST00000338206.5:c.310_311del ENSP00000341045.5:p.Asn104TyrfsTer18
ENST00000616841.4:c.310_311del ENSP00000482004.1:p.Asn104TyrfsTer18
NM_001076.3:c.310_311del NP_001067.2:p.Asn104TyrfsTer18
NM_001076.4:c.310_311del MANE Select NP_001067.2:p.Asn104TyrfsTer18
Search 100 bp 5'
Search 100 bp 3'