Canonical Allele Identifier: CA2263371739

Gene: IGF2BP1

Linked Data

• dbSNP Id: rs2041504365

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49002980A>C , CM000679.2:g.49002980A>C	GRCh38
NC_000017.10:g.47080342A>C , CM000679.1:g.47080342A>C	GRCh37
NC_000017.9:g.44435341A>C	NCBI36
NG_030585.1:g.10569A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000290341.8:c.236+3811A>C MANE Select	ENSP00000290341.3:n.236+3811A>C
ENST00000290341.7:c.236+3811A>C	ENSP00000290341.3:n.236+3811A>C
ENST00000431824.2:c.236+3811A>C	ENSP00000389135.2:n.236+3811A>C
ENST00000510023.5:n.497-1621A>C
ENST00000515586.5:n.219+3811A>C
NM_001160423.1:c.236+3811A>C	NP_001153895.1:n.236+3811A>C
NM_006546.3:c.236+3811A>C	NP_006537.3:n.236+3811A>C
XM_011524201.1:c.236+3811A>C	XP_011522503.1:n.236+3811A>C
XM_011524201.2:c.236+3811A>C	XP_011522503.1:n.236+3811A>C
XM_017024022.1:c.236+3811A>C	XP_016879511.1:n.236+3811A>C
NM_006546.4:c.236+3811A>C MANE Select	NP_006537.3:n.236+3811A>C
NM_001160423.2:c.236+3811A>C	NP_001153895.1:n.236+3811A>C