Canonical Allele Identifier: CA379118067

Gene: IGF2 INS-IGF2

Linked Data

• MyVariant Identifiers: chr11:g.2170377G>A (hg19) ; chr11:g.2149147G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2149147G>A , CM000673.2:g.2149147G>A	GRCh38
NC_000011.9:g.2170377G>A , CM000673.1:g.2170377G>A	GRCh37
NC_000011.8:g.2126953G>A	NCBI36
NG_008849.1:g.5457C>T
NG_050578.1:g.17063C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481781.3:c.-270C>T (IGF2)	ENSP00000511998.1:n.-270C>T
ENST00000643349.2:c.233C>T	ENSP00000495715.1:p.Thr78Ile
ENST00000695541.1:c.-270C>T (IGF2)	ENSP00000511997.1:n.-270C>T
ENST00000481781.2:n.324C>T
ENST00000643349.1:c.233C>T	ENSP00000495715.1:p.Thr78Ile
ENST00000356578.8:c.386C>T (INS-IGF2)	ENSP00000348986.4:p.Thr129Ile
ENST00000397270.1:c.386C>T (INS-IGF2)	ENSP00000380440.1:p.Thr129Ile
ENST00000476874.1:n.269C>T (INS-IGF2)
ENST00000481781.1:n.591C>T (INS-IGF2)
NM_001007139.5:c.-270C>T (IGF2)	NP_001007140.2:n.-270C>T
NM_001042376.2:c.386C>T (INS-IGF2)	NP_001035835.1:p.Thr129Ile
NR_003512.3:n.445C>T (INS-IGF2)
NM_001042376.3:c.386C>T (INS-IGF2)	NP_001035835.1:p.Thr129Ile
NR_003512.4:n.445C>T (INS-IGF2)
NM_001007139.6:c.-270C>T (IGF2)	NP_001007140.2:n.-270C>T