Canonical Allele Identifier: CA1063776686

Gene: UGT2B10

Linked Data

• dbSNP Id: rs1737242983
• gnomAD v3: 4-68816920-G-GAA
• gnomAD v4: 4-68816920-G-GAA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68816923_68816924dup , CM000666.2:g.68816923_68816924dup	GRCh38
NC_000004.11:g.69682641_69682642dup , CM000666.1:g.69682641_69682642dup	GRCh37
NC_000004.10:g.69717230_69717231dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265403.12:c.718+186_718+187dup MANE Select	ENSP00000265403.7:n.718+186_718+187dup
ENST00000265403.11:c.718+186_718+187dup	ENSP00000265403.7:n.718+186_718+187dup
ENST00000458688.2:c.466+438_466+439dup	ENSP00000413420.2:n.466+438_466+439dup
NM_001075.5:c.718+186_718+187dup	NP_001066.1:n.718+186_718+187dup
NM_001144767.2:c.466+438_466+439dup	NP_001138239.1:n.466+438_466+439dup
NM_001290091.1:c.-27+751_-27+752dup	NP_001277020.1:n.-27+751_-27+752dup
XM_017008585.2:c.718+186_718+187dup	XP_016864074.1:n.718+186_718+187dup
NM_001075.6:c.718+186_718+187dup MANE Select	NP_001066.1:n.718+186_718+187dup
NM_001144767.3:c.466+438_466+439dup	NP_001138239.1:n.466+438_466+439dup
NM_001290091.2:c.-27+751_-27+752dup	NP_001277020.1:n.-27+751_-27+752dup