Canonical Allele Identifier: CA379118133

Gene: IGF2 INS-IGF2

Linked Data

• MyVariant Identifiers: chr11:g.2170394A>C (hg19) ; chr11:g.2149164A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2149164A>C , CM000673.2:g.2149164A>C	GRCh38
NC_000011.9:g.2170394A>C , CM000673.1:g.2170394A>C	GRCh37
NC_000011.8:g.2126970A>C	NCBI36
NG_008849.1:g.5440T>G
NG_050578.1:g.17046T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481781.3:c.-287T>G (IGF2)	ENSP00000511998.1:n.-287T>G
ENST00000643349.2:c.216T>G	ENSP00000495715.1:p.Cys72Trp
ENST00000695541.1:c.-287T>G (IGF2)	ENSP00000511997.1:n.-287T>G
ENST00000481781.2:n.307T>G
ENST00000643349.1:c.216T>G	ENSP00000495715.1:p.Cys72Trp
ENST00000356578.8:c.369T>G (INS-IGF2)	ENSP00000348986.4:p.Cys123Trp
ENST00000397270.1:c.369T>G (INS-IGF2)	ENSP00000380440.1:p.Cys123Trp
ENST00000476874.1:n.252T>G (INS-IGF2)
ENST00000481781.1:n.574T>G (INS-IGF2)
NM_001007139.5:c.-287T>G (IGF2)	NP_001007140.2:n.-287T>G
NM_001042376.2:c.369T>G (INS-IGF2)	NP_001035835.1:p.Cys123Trp
NR_003512.3:n.428T>G (INS-IGF2)
NM_001042376.3:c.369T>G (INS-IGF2)	NP_001035835.1:p.Cys123Trp
NR_003512.4:n.428T>G (INS-IGF2)
NM_001007139.6:c.-287T>G (IGF2)	NP_001007140.2:n.-287T>G