Canonical Allele Identifier: CA379118640

Gene: IGF2 INS-IGF2

Linked Data

• MyVariant Identifiers: chr11:g.2170530C>G (hg19) ; chr11:g.2149300C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2149300C>G , CM000673.2:g.2149300C>G	GRCh38
NC_000011.9:g.2170530C>G , CM000673.1:g.2170530C>G	GRCh37
NC_000011.8:g.2127106C>G	NCBI36
NG_008849.1:g.5304G>C
NG_050578.1:g.16910G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481781.3:c.-423G>C (IGF2)	ENSP00000511998.1:n.-423G>C
ENST00000643349.2:c.80G>C	ENSP00000495715.1:p.Gly27Ala
ENST00000695541.1:c.-423G>C (IGF2)	ENSP00000511997.1:n.-423G>C
ENST00000481781.2:n.171G>C
ENST00000643349.1:c.80G>C	ENSP00000495715.1:p.Gly27Ala
ENST00000356578.8:c.233G>C (INS-IGF2)	ENSP00000348986.4:p.Gly78Ala
ENST00000397270.1:c.233G>C (INS-IGF2)	ENSP00000380440.1:p.Gly78Ala
ENST00000476874.1:n.116G>C (INS-IGF2)
ENST00000481781.1:n.438G>C (INS-IGF2)
NM_001007139.5:c.-423G>C (IGF2)	NP_001007140.2:n.-423G>C
NM_001042376.2:c.233G>C (INS-IGF2)	NP_001035835.1:p.Gly78Ala
NR_003512.3:n.292G>C (INS-IGF2)
NM_001042376.3:c.233G>C (INS-IGF2)	NP_001035835.1:p.Gly78Ala
NR_003512.4:n.292G>C (INS-IGF2)
NM_001007139.6:c.-423G>C (IGF2)	NP_001007140.2:n.-423G>C