Canonical Allele Identifier: CA2263371733

Gene: IGF2BP1

Linked Data

• dbSNP Id: rs2041504288

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49002970A>G , CM000679.2:g.49002970A>G	GRCh38
NC_000017.10:g.47080332A>G , CM000679.1:g.47080332A>G	GRCh37
NC_000017.9:g.44435331A>G	NCBI36
NG_030585.1:g.10559A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000290341.8:c.236+3801A>G MANE Select	ENSP00000290341.3:n.236+3801A>G
ENST00000290341.7:c.236+3801A>G	ENSP00000290341.3:n.236+3801A>G
ENST00000431824.2:c.236+3801A>G	ENSP00000389135.2:n.236+3801A>G
ENST00000510023.5:n.497-1631A>G
ENST00000515586.5:n.219+3801A>G
NM_001160423.1:c.236+3801A>G	NP_001153895.1:n.236+3801A>G
NM_006546.3:c.236+3801A>G	NP_006537.3:n.236+3801A>G
XM_011524201.1:c.236+3801A>G	XP_011522503.1:n.236+3801A>G
XM_011524201.2:c.236+3801A>G	XP_011522503.1:n.236+3801A>G
XM_017024022.1:c.236+3801A>G	XP_016879511.1:n.236+3801A>G
NM_006546.4:c.236+3801A>G MANE Select	NP_006537.3:n.236+3801A>G
NM_001160423.2:c.236+3801A>G	NP_001153895.1:n.236+3801A>G