Canonical Allele Identifier: CA2670844505
Gene: UGT2B15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68669768_68669770del , CM000666.2:g.68669768_68669770del GRCh38
NC_000004.11:g.69535486_69535488del , CM000666.1:g.69535486_69535488del GRCh37
NC_000004.10:g.69218081_69218083del NCBI36
NG_052676.1:g.6010_6012del

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.724+128_724+130del MANE Select ENSP00000341045.5:n.724+128_724+130del
ENST00000338206.5:c.724+128_724+130del ENSP00000341045.5:n.724+128_724+130del
ENST00000616841.4:c.724+128_724+130del ENSP00000482004.1:n.724+128_724+130del
NM_001076.3:c.724+128_724+130del NP_001067.2:n.724+128_724+130del
NM_001076.4:c.724+128_724+130del MANE Select NP_001067.2:n.724+128_724+130del