Canonical Allele Identifier: CA1465793568

Gene: UGT2B15

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68669850A= , CM000666.2:g.68669850A=	GRCh38
NC_000004.11:g.69535568A= , CM000666.1:g.69535568A=	GRCh37
NC_000004.10:g.69218163A=	NCBI36
NG_052676.1:g.5927T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.724+45T= MANE Select	ENSP00000341045.5:n.724+45T=
ENST00000338206.5:c.724+45T=	ENSP00000341045.5:n.724+45T=
ENST00000616841.4:c.724+45T=	ENSP00000482004.1:n.724+45T=
NM_001076.3:c.724+45T=	NP_001067.2:n.724+45T=
NM_001076.4:c.724+45T= MANE Select	NP_001067.2:n.724+45T=