Canonical Allele Identifier: CA772686620

Gene: IGF2BP1

Linked Data

• dbSNP Id: rs1417352530
• gnomAD v3: 17-49003040-T-A
• gnomAD v4: 17-49003040-T-A
• MyVariant Identifiers: chr17:g.47080402T>A (hg19) ; chr17:g.49003040T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49003040T>A , CM000679.2:g.49003040T>A	GRCh38
NC_000017.10:g.47080402T>A , CM000679.1:g.47080402T>A	GRCh37
NC_000017.9:g.44435401T>A	NCBI36
NG_030585.1:g.10629T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000290341.8:c.236+3871T>A MANE Select	ENSP00000290341.3:n.236+3871T>A
ENST00000290341.7:c.236+3871T>A	ENSP00000290341.3:n.236+3871T>A
ENST00000431824.2:c.236+3871T>A	ENSP00000389135.2:n.236+3871T>A
ENST00000510023.5:n.497-1561T>A
ENST00000515586.5:n.219+3871T>A
NM_001160423.1:c.236+3871T>A	NP_001153895.1:n.236+3871T>A
NM_006546.3:c.236+3871T>A	NP_006537.3:n.236+3871T>A
XM_011524201.1:c.236+3871T>A	XP_011522503.1:n.236+3871T>A
XM_011524201.2:c.236+3871T>A	XP_011522503.1:n.236+3871T>A
XM_017024022.1:c.236+3871T>A	XP_016879511.1:n.236+3871T>A
NM_006546.4:c.236+3871T>A MANE Select	NP_006537.3:n.236+3871T>A
NM_001160423.2:c.236+3871T>A	NP_001153895.1:n.236+3871T>A