Canonical Allele Identifier: CA379118804

Gene: IGF2 INS-IGF2

Linked Data

• MyVariant Identifiers: chr11:g.2170566A>C (hg19) ; chr11:g.2149336A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2149336A>C , CM000673.2:g.2149336A>C	GRCh38
NC_000011.9:g.2170566A>C , CM000673.1:g.2170566A>C	GRCh37
NC_000011.8:g.2127142A>C	NCBI36
NG_008849.1:g.5268T>G
NG_050578.1:g.16874T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481781.3:c.-459T>G (IGF2)	ENSP00000511998.1:n.-459T>G
ENST00000643349.2:c.44T>G	ENSP00000495715.1:p.Leu15Trp
ENST00000695541.1:c.-459T>G (IGF2)	ENSP00000511997.1:n.-459T>G
ENST00000481781.2:n.135T>G
ENST00000643349.1:c.44T>G	ENSP00000495715.1:p.Leu15Trp
ENST00000356578.8:c.197T>G (INS-IGF2)	ENSP00000348986.4:p.Leu66Trp
ENST00000397270.1:c.197T>G (INS-IGF2)	ENSP00000380440.1:p.Leu66Trp
ENST00000476874.1:n.80T>G (INS-IGF2)
ENST00000481781.1:n.402T>G (INS-IGF2)
NM_001007139.5:c.-459T>G (IGF2)	NP_001007140.2:n.-459T>G
NM_001042376.2:c.197T>G (INS-IGF2)	NP_001035835.1:p.Leu66Trp
NR_003512.3:n.256T>G (INS-IGF2)
NM_001042376.3:c.197T>G (INS-IGF2)	NP_001035835.1:p.Leu66Trp
NR_003512.4:n.256T>G (INS-IGF2)
NM_001007139.6:c.-459T>G (IGF2)	NP_001007140.2:n.-459T>G