Canonical Allele Identifier: CA1465820879

Gene: UGT2B15

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68646912A= , CM000666.2:g.68646912A=	GRCh38
NC_000004.11:g.69512630A= , CM000666.1:g.69512630A=	GRCh37
NC_000004.10:g.69195225A=	NCBI36
NG_052676.1:g.28865T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.*192T= MANE Select	ENSP00000341045.5:n.*192T=
ENST00000338206.5:c.*192T=	ENSP00000341045.5:n.*192T=
ENST00000616841.4:c.1732+53T=	ENSP00000482004.1:n.1732+53T=
NM_001076.3:c.*192T=	NP_001067.2:n.*192T=
NM_001076.4:c.*192T= MANE Select	NP_001067.2:n.*192T=