Canonical Allele Identifier: CA1465793503

Gene: UGT2B15

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68669783T= , CM000666.2:g.68669783T=	GRCh38
NC_000004.11:g.69535501T= , CM000666.1:g.69535501T=	GRCh37
NC_000004.10:g.69218096T=	NCBI36
NG_052676.1:g.5994A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.724+112A= MANE Select	ENSP00000341045.5:n.724+112A=
ENST00000338206.5:c.724+112A=	ENSP00000341045.5:n.724+112A=
ENST00000616841.4:c.724+112A=	ENSP00000482004.1:n.724+112A=
NM_001076.3:c.724+112A=	NP_001067.2:n.724+112A=
NM_001076.4:c.724+112A= MANE Select	NP_001067.2:n.724+112A=