Canonical Allele Identifier: CA1465794158

Gene: UGT2B15

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68670184C= , CM000666.2:g.68670184C=	GRCh38
NC_000004.11:g.69535902C= , CM000666.1:g.69535902C=	GRCh37
NC_000004.10:g.69218497C=	NCBI36
NG_052676.1:g.5593G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000338206.6:c.435G= MANE Select	ENSP00000341045.5:p.Lys145=
ENST00000338206.5:c.435G=	ENSP00000341045.5:p.Lys145=
ENST00000616841.4:c.435G=	ENSP00000482004.1:p.Lys145=
NM_001076.3:c.435G=	NP_001067.2:p.Lys145=
NM_001076.4:c.435G= MANE Select	NP_001067.2:p.Lys145=