Canonical Allele Identifier: CA2706294238

Gene: UGT2B15

Linked Data

• dbSNP Id: rs2109838064

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68669768_68669769dup , CM000666.2:g.68669768_68669769dup	GRCh38
NC_000004.11:g.69535486_69535487dup , CM000666.1:g.69535486_69535487dup	GRCh37
NC_000004.10:g.69218081_69218082dup	NCBI36
NG_052676.1:g.6008_6009dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.724+126_724+127dup MANE Select	ENSP00000341045.5:n.724+126_724+127dup
ENST00000338206.5:c.724+126_724+127dup	ENSP00000341045.5:n.724+126_724+127dup
ENST00000616841.4:c.724+126_724+127dup	ENSP00000482004.1:n.724+126_724+127dup
NM_001076.3:c.724+126_724+127dup	NP_001067.2:n.724+126_724+127dup
NM_001076.4:c.724+126_724+127dup MANE Select	NP_001067.2:n.724+126_724+127dup