Canonical Allele Identifier: CA1465820983

Gene: UGT2B15

Linked Data

• dbSNP Id: rs1732496954

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68647100_68647108dup , CM000666.2:g.68647100_68647108dup	GRCh38
NC_000004.11:g.69512818_69512826dup , CM000666.1:g.69512818_69512826dup	GRCh37
NC_000004.10:g.69195413_69195421dup	NCBI36
NG_052676.1:g.28671_28679dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.1591_*6dup MANE Select	ENSP00000341045.5:n.1591_*6dup
ENST00000338206.5:c.1591_*6dup	ENSP00000341045.5:n.1591_*6dup
ENST00000616841.4:c.1591_1599dup	ENSP00000482004.1:n.1591_1599dup
NM_001076.3:c.1591_*6dup	NP_001067.2:n.1591_*6dup
NM_001076.4:c.1591_*6dup MANE Select	NP_001067.2:n.1591_*6dup