Canonical Allele Identifier: CA472029154

Gene: IGF2 INS-IGF2

Linked Data

• dbSNP Id: rs1395473757
• gnomAD v2: 11-2170421-A-G
• gnomAD v4: 11-2149191-A-G
• MyVariant Identifiers: chr11:g.2170421A>G (hg19) ; chr11:g.2149191A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2149191A>G , CM000673.2:g.2149191A>G	GRCh38
NC_000011.9:g.2170421A>G , CM000673.1:g.2170421A>G	GRCh37
NC_000011.8:g.2126997A>G	NCBI36
NG_008849.1:g.5413T>C
NG_050578.1:g.17019T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481781.3:c.-314T>C (IGF2)	ENSP00000511998.1:n.-314T>C
ENST00000643349.2:c.189T>C	ENSP00000495715.1:p.Ser63=
ENST00000695541.1:c.-314T>C (IGF2)	ENSP00000511997.1:n.-314T>C
ENST00000481781.2:n.280T>C
ENST00000643349.1:c.189T>C	ENSP00000495715.1:p.Ser63=
ENST00000356578.8:c.342T>C (INS-IGF2)	ENSP00000348986.4:p.Ser114=
ENST00000397270.1:c.342T>C (INS-IGF2)	ENSP00000380440.1:p.Ser114=
ENST00000476874.1:n.225T>C (INS-IGF2)
ENST00000481781.1:n.547T>C (INS-IGF2)
NM_001007139.5:c.-314T>C (IGF2)	NP_001007140.2:n.-314T>C
NM_001042376.2:c.342T>C (INS-IGF2)	NP_001035835.1:p.Ser114=
NR_003512.3:n.401T>C (INS-IGF2)
NM_001042376.3:c.342T>C (INS-IGF2)	NP_001035835.1:p.Ser114=
NR_003512.4:n.401T>C (INS-IGF2)
NM_001007139.6:c.-314T>C (IGF2)	NP_001007140.2:n.-314T>C