Canonical Allele Identifier: CA1465793598
Gene: UGT2B15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68669874C= , CM000666.2:g.68669874C= GRCh38
NC_000004.11:g.69535592C= , CM000666.1:g.69535592C= GRCh37
NC_000004.10:g.69218187C= NCBI36
NG_052676.1:g.5903G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.724+21G= MANE Select ENSP00000341045.5:n.724+21G=
ENST00000338206.5:c.724+21G= ENSP00000341045.5:n.724+21G=
ENST00000616841.4:c.724+21G= ENSP00000482004.1:n.724+21G=
NM_001076.3:c.724+21G= NP_001067.2:n.724+21G=
NM_001076.4:c.724+21G= MANE Select NP_001067.2:n.724+21G=