Canonical Allele Identifier: CA1057348898

Gene: IGF2BP2

Linked Data

• dbSNP Id: rs1739769464
• gnomAD v3: 3-185811164-G-GAAAAAATAATTATTATTTTATTAATAGGTA
• gnomAD v4: 3-185811164-G-GAAAAAATAATTATTATTTTATTAATAGGTA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.185811168_185811197dup , CM000665.2:g.185811168_185811197dup	GRCh38
NC_000003.11:g.185528956_185528985dup , CM000665.1:g.185528956_185528985dup	GRCh37
NC_000003.10:g.187011650_187011679dup	NCBI36
NG_011602.1:g.18846_18875dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000382199.7:c.239+11959_239+11988dup MANE Select	ENSP00000371634.3:n.239+11959_239+11988du...
ENST00000346192.7:c.239+11959_239+11988dup	ENSP00000320204.5:n.239+11959_239+11988du...
ENST00000382199.6:c.239+11959_239+11988dup	ENSP00000371634.2:n.239+11959_239+11988du...
ENST00000421047.3:c.50+9818_50+9847dup	ENSP00000413787.3:n.50+9818_50+9847dup
ENST00000457616.6:c.239+11959_239+11988dup	ENSP00000410242.2:n.239+11959_239+11988du...
ENST00000461957.5:n.119+11959_119+11988dup
ENST00000466476.1:n.171+11959_171+11988dup
ENST00000493302.5:n.120+9818_120+9847dup
NM_001007225.1:c.239+11959_239+11988dup	NP_001007226.1:n.239+11959_239+11988dup
NM_001291869.1:c.239+11959_239+11988dup	NP_001278798.1:n.239+11959_239+11988dup
NM_001291872.1:c.50+9818_50+9847dup	NP_001278801.1:n.50+9818_50+9847dup
NM_001291873.1:c.50+9818_50+9847dup	NP_001278802.1:n.50+9818_50+9847dup
NM_001291874.1:c.50+9818_50+9847dup	NP_001278803.1:n.50+9818_50+9847dup
NM_001291875.1:c.-106+9818_-106+9847dup	NP_001278804.1:n.-106+9818_-106+9847dup
NM_006548.4:c.239+11959_239+11988dup	NP_006539.3:n.239+11959_239+11988dup
XM_011512338.1:c.239+11959_239+11988dup	XP_011510640.1:n.239+11959_239+11988dup
XM_011512339.1:c.239+11959_239+11988dup	XP_011510641.1:n.239+11959_239+11988dup
XM_011512341.1:c.239+11959_239+11988dup	XP_011510643.1:n.239+11959_239+11988dup
XR_427358.2:n.318+11959_318+11988dup
NM_001007225.2:c.239+11959_239+11988dup	NP_001007226.1:n.239+11959_239+11988dup
NM_001291869.2:c.239+11959_239+11988dup	NP_001278798.1:n.239+11959_239+11988dup
NM_001291872.2:c.50+9818_50+9847dup	NP_001278801.1:n.50+9818_50+9847dup
NM_001291873.2:c.50+9818_50+9847dup	NP_001278802.1:n.50+9818_50+9847dup
NM_001291874.2:c.50+9818_50+9847dup	NP_001278803.1:n.50+9818_50+9847dup
NM_001291875.2:c.-106+9818_-106+9847dup	NP_001278804.1:n.-106+9818_-106+9847dup
NM_006548.5:c.239+11959_239+11988dup	NP_006539.3:n.239+11959_239+11988dup
NR_138486.1:n.335+11959_335+11988dup
XM_017005557.2:c.178+13589_178+13618dup	XP_016861046.1:n.178+13589_178+13618dup
XM_017005558.2:c.239+11959_239+11988dup	XP_016861047.1:n.239+11959_239+11988dup
XM_017005559.2:c.239+11959_239+11988dup	XP_016861048.1:n.239+11959_239+11988dup
XM_017005560.2:c.35+11959_35+11988dup	XP_016861049.1:n.35+11959_35+11988dup
XM_017005561.1:c.239+11959_239+11988dup	XP_016861050.1:n.239+11959_239+11988dup
XM_017005562.1:c.239+11959_239+11988dup	XP_016861051.1:n.239+11959_239+11988dup
XM_017005563.1:c.239+11959_239+11988dup	XP_016861052.1:n.239+11959_239+11988dup
XM_017005564.1:c.239+11959_239+11988dup	XP_016861053.1:n.239+11959_239+11988dup
XM_024453316.1:c.-170+13589_-170+13618dup	XP_024309084.1:n.-170+13589_-170+13618dup...
XR_001739984.2:n.324+11959_324+11988dup
NM_001007225.3:c.239+11959_239+11988dup	NP_001007226.1:n.239+11959_239+11988dup
NM_001291869.3:c.239+11959_239+11988dup	NP_001278798.1:n.239+11959_239+11988dup
NM_001291872.3:c.50+9818_50+9847dup	NP_001278801.1:n.50+9818_50+9847dup
NM_001291874.3:c.50+9818_50+9847dup	NP_001278803.1:n.50+9818_50+9847dup
NM_001291875.3:c.-106+9818_-106+9847dup	NP_001278804.1:n.-106+9818_-106+9847dup
NM_006548.6:c.239+11959_239+11988dup MANE Select	NP_006539.3:n.239+11959_239+11988dup
NR_138486.2:n.321+11959_321+11988dup
NM_001291873.3:c.50+9818_50+9847dup	NP_001278802.1:n.50+9818_50+9847dup