Canonical Allele Identifier: CA2943013

Gene: UGT2B10

Linked Data

• dbSNP Id: rs772834799
• ExAC: 4:69682484 AGC / A
• gnomAD v2: 4-69682484-AGC-A
• gnomAD v3: 4-68816766-AGC-A
• gnomAD v4: 4-68816766-AGC-A
• MyVariant Identifiers: chr4:g.69682485_69682486del (hg19) ; chr4:g.68816767_68816768del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68816767_68816768del , CM000666.2:g.68816767_68816768del	GRCh38
NC_000004.11:g.69682485_69682486del , CM000666.1:g.69682485_69682486del	GRCh37
NC_000004.10:g.69717074_69717075del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265403.12:c.718+30_718+31del MANE Select	ENSP00000265403.7:n.718+30_718+31del
ENST00000265403.11:c.718+30_718+31del	ENSP00000265403.7:n.718+30_718+31del
ENST00000458688.2:c.466+282_466+283del	ENSP00000413420.2:n.466+282_466+283del
NM_001075.5:c.718+30_718+31del	NP_001066.1:n.718+30_718+31del
NM_001144767.2:c.466+282_466+283del	NP_001138239.1:n.466+282_466+283del
NM_001290091.1:c.-27+595_-27+596del	NP_001277020.1:n.-27+595_-27+596del
XM_017008585.2:c.718+30_718+31del	XP_016864074.1:n.718+30_718+31del
NM_001075.6:c.718+30_718+31del MANE Select	NP_001066.1:n.718+30_718+31del
NM_001144767.3:c.466+282_466+283del	NP_001138239.1:n.466+282_466+283del
NM_001290091.2:c.-27+595_-27+596del	NP_001277020.1:n.-27+595_-27+596del