Canonical Allele Identifier: CA597431531

Gene: IGF2 INS-IGF2 IGF2-AS

Linked Data

• dbSNP Id: rs1156608663
• gnomAD v2: 11-2167472-C-G
• gnomAD v4: 11-2146242-C-G
• MyVariant Identifiers: chr11:g.2167472C>G (hg19) ; chr11:g.2146242C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2146242C>G , CM000673.2:g.2146242C>G	GRCh38
NC_000011.9:g.2167472C>G , CM000673.1:g.2167472C>G	GRCh37
NC_000011.8:g.2124048C>G	NCBI36
NG_008849.1:g.8362G>C
NG_050578.1:g.19968G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000481781.3:c.-7+1324G>C (IGF2)	ENSP00000511998.1:n.-7+1324G>C
ENST00000643349.2:c.*46+1324G>C	ENSP00000495715.1:n.*46+1324G>C
ENST00000695541.1:c.-7+1324G>C (IGF2)	ENSP00000511997.1:n.-7+1324G>C
ENST00000643349.1:c.*46+1324G>C	ENSP00000495715.1:n.*46+1324G>C
ENST00000356578.8:c.*46+1324G>C (INS-IGF2)	ENSP00000348986.4:n.*46+1324G>C
NM_001007139.5:c.-7+1324G>C (IGF2)	NP_001007140.2:n.-7+1324G>C
NR_003512.3:n.708+1324G>C (INS-IGF2)
NR_028043.2:n.437-3C>G (IGF2-AS)
NR_133657.1:n.437-114C>G (IGF2-AS)
NR_003512.4:n.708+1324G>C (INS-IGF2)
NM_001007139.6:c.-7+1324G>C (IGF2)	NP_001007140.2:n.-7+1324G>C