Canonical Allele Identifier: CA472029264
Gene: IGF2 HGNC NCBI
INS-IGF2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.2170454G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2149224G>C , CM000673.2:g.2149224G>C GRCh38
NC_000011.9:g.2170454G>C , CM000673.1:g.2170454G>C GRCh37
NC_000011.8:g.2127030G>C NCBI36
NG_008849.1:g.5380C>G
NG_050578.1:g.16986C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000481781.3:c.-347C>G (IGF2) ENSP00000511998.1:n.-347C>G
ENST00000643349.2:c.156C>G ENSP00000495715.1:p.Ser52=
ENST00000695541.1:c.-347C>G (IGF2) ENSP00000511997.1:n.-347C>G
ENST00000481781.2:n.247C>G
ENST00000643349.1:c.156C>G ENSP00000495715.1:p.Ser52=
ENST00000356578.8:c.309C>G (INS-IGF2) ENSP00000348986.4:p.Ser103=
ENST00000397270.1:c.309C>G (INS-IGF2) ENSP00000380440.1:p.Ser103=
ENST00000476874.1:n.192C>G (INS-IGF2)
ENST00000481781.1:n.514C>G (INS-IGF2)
NM_001007139.5:c.-347C>G (IGF2) NP_001007140.2:n.-347C>G
NM_001042376.2:c.309C>G (INS-IGF2) NP_001035835.1:p.Ser103=
NR_003512.3:n.368C>G (INS-IGF2)
NM_001042376.3:c.309C>G (INS-IGF2) NP_001035835.1:p.Ser103=
NR_003512.4:n.368C>G (INS-IGF2)
NM_001007139.6:c.-347C>G (IGF2) NP_001007140.2:n.-347C>G