Canonical Allele Identifier: CA1465820868

Gene: UGT2B15

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68646886C= , CM000666.2:g.68646886C=	GRCh38
NC_000004.11:g.69512604C= , CM000666.1:g.69512604C=	GRCh37
NC_000004.10:g.69195199C=	NCBI36
NG_052676.1:g.28891G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.*218G= MANE Select	ENSP00000341045.5:n.*218G=
ENST00000338206.5:c.*218G=	ENSP00000341045.5:n.*218G=
ENST00000616841.4:c.1732+79G=	ENSP00000482004.1:n.1732+79G=
NM_001076.3:c.*218G=	NP_001067.2:n.*218G=
NM_001076.4:c.*218G= MANE Select	NP_001067.2:n.*218G=