Canonical Allele Identifier: CA2670847362

Gene: UGT2B10

Linked Data

• gnomAD v4: 4-68816783-G-GCC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68816783_68816784insCC , CM000666.2:g.68816783_68816784insCC	GRCh38
NC_000004.11:g.69682501_69682502insCC , CM000666.1:g.69682501_69682502insCC	GRCh37
NC_000004.10:g.69717090_69717091insCC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265403.12:c.718+46_718+47insCC MANE Select	ENSP00000265403.7:n.718+46_718+47insCC
ENST00000265403.11:c.718+46_718+47insCC	ENSP00000265403.7:n.718+46_718+47insCC
ENST00000458688.2:c.466+298_466+299insCC	ENSP00000413420.2:n.466+298_466+299insCC
NM_001075.5:c.718+46_718+47insCC	NP_001066.1:n.718+46_718+47insCC
NM_001144767.2:c.466+298_466+299insCC	NP_001138239.1:n.466+298_466+299insCC
NM_001290091.1:c.-27+611_-27+612insCC	NP_001277020.1:n.-27+611_-27+612insCC
XM_017008585.2:c.718+46_718+47insCC	XP_016864074.1:n.718+46_718+47insCC
NM_001075.6:c.718+46_718+47insCC MANE Select	NP_001066.1:n.718+46_718+47insCC
NM_001144767.3:c.466+298_466+299insCC	NP_001138239.1:n.466+298_466+299insCC
NM_001290091.2:c.-27+611_-27+612insCC	NP_001277020.1:n.-27+611_-27+612insCC