Canonical Allele Identifier: CA379118096

Gene: IGF2 INS-IGF2

Linked Data

• dbSNP Id: rs1860164447
• MyVariant Identifiers: chr11:g.2170386G>T (hg19) ; chr11:g.2149156G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2149156G>T , CM000673.2:g.2149156G>T	GRCh38
NC_000011.9:g.2170386G>T , CM000673.1:g.2170386G>T	GRCh37
NC_000011.8:g.2126962G>T	NCBI36
NG_008849.1:g.5448C>A
NG_050578.1:g.17054C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481781.3:c.-279C>A (IGF2)	ENSP00000511998.1:n.-279C>A
ENST00000643349.2:c.224C>A	ENSP00000495715.1:p.Ala75Asp
ENST00000695541.1:c.-279C>A (IGF2)	ENSP00000511997.1:n.-279C>A
ENST00000481781.2:n.315C>A
ENST00000643349.1:c.224C>A	ENSP00000495715.1:p.Ala75Asp
ENST00000356578.8:c.377C>A (INS-IGF2)	ENSP00000348986.4:p.Ala126Asp
ENST00000397270.1:c.377C>A (INS-IGF2)	ENSP00000380440.1:p.Ala126Asp
ENST00000476874.1:n.260C>A (INS-IGF2)
ENST00000481781.1:n.582C>A (INS-IGF2)
NM_001007139.5:c.-279C>A (IGF2)	NP_001007140.2:n.-279C>A
NM_001042376.2:c.377C>A (INS-IGF2)	NP_001035835.1:p.Ala126Asp
NR_003512.3:n.436C>A (INS-IGF2)
NM_001042376.3:c.377C>A (INS-IGF2)	NP_001035835.1:p.Ala126Asp
NR_003512.4:n.436C>A (INS-IGF2)
NM_001007139.6:c.-279C>A (IGF2)	NP_001007140.2:n.-279C>A