Canonical Allele Identifier: CA1426641943

Gene: IGF2BP2

Linked Data

• dbSNP Id: rs1736981196

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.185793957dup , CM000665.2:g.185793957dup	GRCh38
NC_000003.11:g.185511745dup , CM000665.1:g.185511745dup	GRCh37
NC_000003.10:g.186994439dup	NCBI36
NG_011602.1:g.36084dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000382199.7:c.239+29197dup MANE Select	ENSP00000371634.3:n.239+29197dup
ENST00000346192.7:c.239+29197dup	ENSP00000320204.5:n.239+29197dup
ENST00000382199.6:c.239+29197dup	ENSP00000371634.2:n.239+29197dup
ENST00000421047.3:c.50+27056dup	ENSP00000413787.3:n.50+27056dup
ENST00000457616.6:c.239+29197dup	ENSP00000410242.2:n.239+29197dup
ENST00000461957.5:n.119+29197dup
ENST00000466476.1:n.171+29197dup
ENST00000493302.5:n.120+27056dup
NM_001007225.1:c.239+29197dup	NP_001007226.1:n.239+29197dup
NM_001291869.1:c.239+29197dup	NP_001278798.1:n.239+29197dup
NM_001291872.1:c.50+27056dup	NP_001278801.1:n.50+27056dup
NM_001291873.1:c.50+27056dup	NP_001278802.1:n.50+27056dup
NM_001291874.1:c.50+27056dup	NP_001278803.1:n.50+27056dup
NM_001291875.1:c.-106+27056dup	NP_001278804.1:n.-106+27056dup
NM_006548.4:c.239+29197dup	NP_006539.3:n.239+29197dup
XM_011512338.1:c.239+29197dup	XP_011510640.1:n.239+29197dup
XM_011512339.1:c.239+29197dup	XP_011510641.1:n.239+29197dup
XM_011512341.1:c.239+29197dup	XP_011510643.1:n.239+29197dup
XR_427358.2:n.318+29197dup
NM_001007225.2:c.239+29197dup	NP_001007226.1:n.239+29197dup
NM_001291869.2:c.239+29197dup	NP_001278798.1:n.239+29197dup
NM_001291872.2:c.50+27056dup	NP_001278801.1:n.50+27056dup
NM_001291873.2:c.50+27056dup	NP_001278802.1:n.50+27056dup
NM_001291874.2:c.50+27056dup	NP_001278803.1:n.50+27056dup
NM_001291875.2:c.-106+27056dup	NP_001278804.1:n.-106+27056dup
NM_006548.5:c.239+29197dup	NP_006539.3:n.239+29197dup
NR_138486.1:n.335+29197dup
XM_017005557.2:c.178+30827dup	XP_016861046.1:n.178+30827dup
XM_017005558.2:c.239+29197dup	XP_016861047.1:n.239+29197dup
XM_017005559.2:c.239+29197dup	XP_016861048.1:n.239+29197dup
XM_017005560.2:c.35+29197dup	XP_016861049.1:n.35+29197dup
XM_017005561.1:c.239+29197dup	XP_016861050.1:n.239+29197dup
XM_017005562.1:c.239+29197dup	XP_016861051.1:n.239+29197dup
XM_017005563.1:c.239+29197dup	XP_016861052.1:n.239+29197dup
XM_017005564.1:c.239+29197dup	XP_016861053.1:n.239+29197dup
XM_024453316.1:c.-170+30827dup	XP_024309084.1:n.-170+30827dup
XR_001739984.2:n.324+29197dup
NM_001007225.3:c.239+29197dup	NP_001007226.1:n.239+29197dup
NM_001291869.3:c.239+29197dup	NP_001278798.1:n.239+29197dup
NM_001291872.3:c.50+27056dup	NP_001278801.1:n.50+27056dup
NM_001291874.3:c.50+27056dup	NP_001278803.1:n.50+27056dup
NM_001291875.3:c.-106+27056dup	NP_001278804.1:n.-106+27056dup
NM_006548.6:c.239+29197dup MANE Select	NP_006539.3:n.239+29197dup
NR_138486.2:n.321+29197dup
NM_001291873.3:c.50+27056dup	NP_001278802.1:n.50+27056dup