Canonical Allele Identifier: CA1465793496

Gene: UGT2B15

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68669774C= , CM000666.2:g.68669774C=	GRCh38
NC_000004.11:g.69535492C= , CM000666.1:g.69535492C=	GRCh37
NC_000004.10:g.69218087C=	NCBI36
NG_052676.1:g.6003G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.724+121G= MANE Select	ENSP00000341045.5:n.724+121G=
ENST00000338206.5:c.724+121G=	ENSP00000341045.5:n.724+121G=
ENST00000616841.4:c.724+121G=	ENSP00000482004.1:n.724+121G=
NM_001076.3:c.724+121G=	NP_001067.2:n.724+121G=
NM_001076.4:c.724+121G= MANE Select	NP_001067.2:n.724+121G=