Canonical Allele Identifier: CA1465820721

Gene: UGT2B15

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68646677G= , CM000666.2:g.68646677G=	GRCh38
NC_000004.11:g.69512395G= , CM000666.1:g.69512395G=	GRCh37
NC_000004.10:g.69194990G=	NCBI36
NG_052676.1:g.29100C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.*427C= MANE Select	ENSP00000341045.5:n.*427C=
ENST00000338206.5:c.*427C=	ENSP00000341045.5:n.*427C=
ENST00000616841.4:c.1732+288C=	ENSP00000482004.1:n.1732+288C=
NM_001076.3:c.*427C=	NP_001067.2:n.*427C=
NM_001076.4:c.*427C= MANE Select	NP_001067.2:n.*427C=