Canonical Allele Identifier: CA379118211

Gene: IGF2 INS-IGF2

Linked Data

• MyVariant Identifiers: chr11:g.2170410A>G (hg19) ; chr11:g.2149180A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2149180A>G , CM000673.2:g.2149180A>G	GRCh38
NC_000011.9:g.2170410A>G , CM000673.1:g.2170410A>G	GRCh37
NC_000011.8:g.2126986A>G	NCBI36
NG_008849.1:g.5424T>C
NG_050578.1:g.17030T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481781.3:c.-303T>C (IGF2)	ENSP00000511998.1:n.-303T>C
ENST00000643349.2:c.200T>C	ENSP00000495715.1:p.Val67Ala
ENST00000695541.1:c.-303T>C (IGF2)	ENSP00000511997.1:n.-303T>C
ENST00000481781.2:n.291T>C
ENST00000643349.1:c.200T>C	ENSP00000495715.1:p.Val67Ala
ENST00000356578.8:c.353T>C (INS-IGF2)	ENSP00000348986.4:p.Val118Ala
ENST00000397270.1:c.353T>C (INS-IGF2)	ENSP00000380440.1:p.Val118Ala
ENST00000476874.1:n.236T>C (INS-IGF2)
ENST00000481781.1:n.558T>C (INS-IGF2)
NM_001007139.5:c.-303T>C (IGF2)	NP_001007140.2:n.-303T>C
NM_001042376.2:c.353T>C (INS-IGF2)	NP_001035835.1:p.Val118Ala
NR_003512.3:n.412T>C (INS-IGF2)
NM_001042376.3:c.353T>C (INS-IGF2)	NP_001035835.1:p.Val118Ala
NR_003512.4:n.412T>C (INS-IGF2)
NM_001007139.6:c.-303T>C (IGF2)	NP_001007140.2:n.-303T>C