Canonical Allele Identifier: CA903841102

Gene: IGF2BP2

Linked Data

• dbSNP Id: rs1200805442
• gnomAD v3: 3-185794159-T-TCTCA
• gnomAD v4: 3-185794159-T-TCTCA
• MyVariant Identifiers: chr3:g.185511947_185511948insCTCA (hg19) ; chr3:g.185794159_185794160insCTCA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.185794162_185794165dup , CM000665.2:g.185794162_185794165dup	GRCh38
NC_000003.11:g.185511950_185511953dup , CM000665.1:g.185511950_185511953dup	GRCh37
NC_000003.10:g.186994644_186994647dup	NCBI36
NG_011602.1:g.35877_35880dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382199.7:c.239+28990_239+28993dup MANE Select	ENSP00000371634.3:n.239+28990_239+28993dup
ENST00000346192.7:c.239+28990_239+28993dup	ENSP00000320204.5:n.239+28990_239+28993dup
ENST00000382199.6:c.239+28990_239+28993dup	ENSP00000371634.2:n.239+28990_239+28993dup
ENST00000421047.3:c.50+26849_50+26852dup	ENSP00000413787.3:n.50+26849_50+26852dup
ENST00000457616.6:c.239+28990_239+28993dup	ENSP00000410242.2:n.239+28990_239+28993dup
ENST00000461957.5:n.119+28990_119+28993dup
ENST00000466476.1:n.171+28990_171+28993dup
ENST00000493302.5:n.120+26849_120+26852dup
NM_001007225.1:c.239+28990_239+28993dup	NP_001007226.1:n.239+28990_239+28993dup
NM_001291869.1:c.239+28990_239+28993dup	NP_001278798.1:n.239+28990_239+28993dup
NM_001291872.1:c.50+26849_50+26852dup	NP_001278801.1:n.50+26849_50+26852dup
NM_001291873.1:c.50+26849_50+26852dup	NP_001278802.1:n.50+26849_50+26852dup
NM_001291874.1:c.50+26849_50+26852dup	NP_001278803.1:n.50+26849_50+26852dup
NM_001291875.1:c.-106+26849_-106+26852dup	NP_001278804.1:n.-106+26849_-106+26852dup
NM_006548.4:c.239+28990_239+28993dup	NP_006539.3:n.239+28990_239+28993dup
XM_011512338.1:c.239+28990_239+28993dup	XP_011510640.1:n.239+28990_239+28993dup
XM_011512339.1:c.239+28990_239+28993dup	XP_011510641.1:n.239+28990_239+28993dup
XM_011512341.1:c.239+28990_239+28993dup	XP_011510643.1:n.239+28990_239+28993dup
XR_427358.2:n.318+28990_318+28993dup
NM_001007225.2:c.239+28990_239+28993dup	NP_001007226.1:n.239+28990_239+28993dup
NM_001291869.2:c.239+28990_239+28993dup	NP_001278798.1:n.239+28990_239+28993dup
NM_001291872.2:c.50+26849_50+26852dup	NP_001278801.1:n.50+26849_50+26852dup
NM_001291873.2:c.50+26849_50+26852dup	NP_001278802.1:n.50+26849_50+26852dup
NM_001291874.2:c.50+26849_50+26852dup	NP_001278803.1:n.50+26849_50+26852dup
NM_001291875.2:c.-106+26849_-106+26852dup	NP_001278804.1:n.-106+26849_-106+26852dup
NM_006548.5:c.239+28990_239+28993dup	NP_006539.3:n.239+28990_239+28993dup
NR_138486.1:n.335+28990_335+28993dup
XM_017005557.2:c.178+30620_178+30623dup	XP_016861046.1:n.178+30620_178+30623dup
XM_017005558.2:c.239+28990_239+28993dup	XP_016861047.1:n.239+28990_239+28993dup
XM_017005559.2:c.239+28990_239+28993dup	XP_016861048.1:n.239+28990_239+28993dup
XM_017005560.2:c.35+28990_35+28993dup	XP_016861049.1:n.35+28990_35+28993dup
XM_017005561.1:c.239+28990_239+28993dup	XP_016861050.1:n.239+28990_239+28993dup
XM_017005562.1:c.239+28990_239+28993dup	XP_016861051.1:n.239+28990_239+28993dup
XM_017005563.1:c.239+28990_239+28993dup	XP_016861052.1:n.239+28990_239+28993dup
XM_017005564.1:c.239+28990_239+28993dup	XP_016861053.1:n.239+28990_239+28993dup
XM_024453316.1:c.-170+30620_-170+30623dup	XP_024309084.1:n.-170+30620_-170+30623dup
XR_001739984.2:n.324+28990_324+28993dup
NM_001007225.3:c.239+28990_239+28993dup	NP_001007226.1:n.239+28990_239+28993dup
NM_001291869.3:c.239+28990_239+28993dup	NP_001278798.1:n.239+28990_239+28993dup
NM_001291872.3:c.50+26849_50+26852dup	NP_001278801.1:n.50+26849_50+26852dup
NM_001291874.3:c.50+26849_50+26852dup	NP_001278803.1:n.50+26849_50+26852dup
NM_001291875.3:c.-106+26849_-106+26852dup	NP_001278804.1:n.-106+26849_-106+26852dup
NM_006548.6:c.239+28990_239+28993dup MANE Select	NP_006539.3:n.239+28990_239+28993dup
NR_138486.2:n.321+28990_321+28993dup
NM_001291873.3:c.50+26849_50+26852dup	NP_001278802.1:n.50+26849_50+26852dup