Canonical Allele Identifier: CA5818073

Gene: IGF2 INS-IGF2

Linked Data

• dbSNP Id: rs185576219
• ExAC: 11:2170616 A / G
• gnomAD v2: 11-2170616-A-G
• gnomAD v3: 11-2149386-A-G
• gnomAD v4: 11-2149386-A-G
• MyVariant Identifiers: chr11:g.2170616A>G (hg19) ; chr11:g.2149386A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2149386A>G , CM000673.2:g.2149386A>G	GRCh38
NC_000011.9:g.2170616A>G , CM000673.1:g.2170616A>G	GRCh37
NC_000011.8:g.2127192A>G	NCBI36
NG_008849.1:g.5218T>C
NG_050578.1:g.16824T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481781.3:c.-468-41T>C (IGF2)	ENSP00000511998.1:n.-468-41T>C
ENST00000643349.2:c.-7T>C	ENSP00000495715.1:n.-7T>C
ENST00000695541.1:c.-468-41T>C (IGF2)	ENSP00000511997.1:n.-468-41T>C
ENST00000481781.2:n.126-41T>C
ENST00000643349.1:c.-7T>C	ENSP00000495715.1:n.-7T>C
ENST00000356578.8:c.188-41T>C (INS-IGF2)	ENSP00000348986.4:n.188-41T>C
ENST00000397270.1:c.188-41T>C (INS-IGF2)	ENSP00000380440.1:n.188-41T>C
ENST00000476874.1:n.71-41T>C (INS-IGF2)
ENST00000481781.1:n.393-41T>C (INS-IGF2)
NM_001007139.5:c.-509T>C (IGF2)	NP_001007140.2:n.-509T>C
NM_001042376.2:c.188-41T>C (INS-IGF2)	NP_001035835.1:n.188-41T>C
NR_003512.3:n.247-41T>C (INS-IGF2)
NM_001042376.3:c.188-41T>C (INS-IGF2)	NP_001035835.1:n.188-41T>C
NR_003512.4:n.247-41T>C (INS-IGF2)
NM_001007139.6:c.-509T>C (IGF2)	NP_001007140.2:n.-509T>C