Canonical Allele Identifier: CA1465820716

Gene: UGT2B15

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68646668C= , CM000666.2:g.68646668C=	GRCh38
NC_000004.11:g.69512386C= , CM000666.1:g.69512386C=	GRCh37
NC_000004.10:g.69194981C=	NCBI36
NG_052676.1:g.29109G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.*436G= MANE Select	ENSP00000341045.5:n.*436G=
ENST00000338206.5:c.*436G=	ENSP00000341045.5:n.*436G=
ENST00000616841.4:c.1732+297G=	ENSP00000482004.1:n.1732+297G=
NM_001076.3:c.*436G=	NP_001067.2:n.*436G=
NM_001076.4:c.*436G= MANE Select	NP_001067.2:n.*436G=