Canonical Allele Identifier: CA472029573

Gene: IGF2 INS-IGF2

Linked Data

• dbSNP Id: rs1590146569
• MyVariant Identifiers: chr11:g.2170571T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2149341T>C , CM000673.2:g.2149341T>C	GRCh38
NC_000011.9:g.2170571T>C , CM000673.1:g.2170571T>C	GRCh37
NC_000011.8:g.2127147T>C	NCBI36
NG_008849.1:g.5263A>G
NG_050578.1:g.16869A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481781.3:c.-464A>G (IGF2)	ENSP00000511998.1:n.-464A>G
ENST00000643349.2:c.39A>G	ENSP00000495715.1:p.Ser13=
ENST00000695541.1:c.-464A>G (IGF2)	ENSP00000511997.1:n.-464A>G
ENST00000481781.2:n.130A>G
ENST00000643349.1:c.39A>G	ENSP00000495715.1:p.Ser13=
ENST00000356578.8:c.192A>G (INS-IGF2)	ENSP00000348986.4:p.Ser64=
ENST00000397270.1:c.192A>G (INS-IGF2)	ENSP00000380440.1:p.Ser64=
ENST00000476874.1:n.75A>G (INS-IGF2)
ENST00000481781.1:n.397A>G (INS-IGF2)
NM_001007139.5:c.-464A>G (IGF2)	NP_001007140.2:n.-464A>G
NM_001042376.2:c.192A>G (INS-IGF2)	NP_001035835.1:p.Ser64=
NR_003512.3:n.251A>G (INS-IGF2)
NM_001042376.3:c.192A>G (INS-IGF2)	NP_001035835.1:p.Ser64=
NR_003512.4:n.251A>G (INS-IGF2)
NM_001007139.6:c.-464A>G (IGF2)	NP_001007140.2:n.-464A>G