Canonical Allele Identifier: CA1465793602
Gene: UGT2B15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68669875C= , CM000666.2:g.68669875C= GRCh38
NC_000004.11:g.69535593C= , CM000666.1:g.69535593C= GRCh37
NC_000004.10:g.69218188C= NCBI36
NG_052676.1:g.5902G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.724+20G= MANE Select ENSP00000341045.5:n.724+20G=
ENST00000338206.5:c.724+20G= ENSP00000341045.5:n.724+20G=
ENST00000616841.4:c.724+20G= ENSP00000482004.1:n.724+20G=
NM_001076.3:c.724+20G= NP_001067.2:n.724+20G=
NM_001076.4:c.724+20G= MANE Select NP_001067.2:n.724+20G=