Canonical Allele Identifier: CA379118805

Gene: IGF2 INS-IGF2

Linked Data

• gnomAD v4: 11-2149336-A-G
• MyVariant Identifiers: chr11:g.2170566A>G (hg19) ; chr11:g.2149336A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2149336A>G , CM000673.2:g.2149336A>G	GRCh38
NC_000011.9:g.2170566A>G , CM000673.1:g.2170566A>G	GRCh37
NC_000011.8:g.2127142A>G	NCBI36
NG_008849.1:g.5268T>C
NG_050578.1:g.16874T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481781.3:c.-459T>C (IGF2)	ENSP00000511998.1:n.-459T>C
ENST00000643349.2:c.44T>C	ENSP00000495715.1:p.Leu15Ser
ENST00000695541.1:c.-459T>C (IGF2)	ENSP00000511997.1:n.-459T>C
ENST00000481781.2:n.135T>C
ENST00000643349.1:c.44T>C	ENSP00000495715.1:p.Leu15Ser
ENST00000356578.8:c.197T>C (INS-IGF2)	ENSP00000348986.4:p.Leu66Ser
ENST00000397270.1:c.197T>C (INS-IGF2)	ENSP00000380440.1:p.Leu66Ser
ENST00000476874.1:n.80T>C (INS-IGF2)
ENST00000481781.1:n.402T>C (INS-IGF2)
NM_001007139.5:c.-459T>C (IGF2)	NP_001007140.2:n.-459T>C
NM_001042376.2:c.197T>C (INS-IGF2)	NP_001035835.1:p.Leu66Ser
NR_003512.3:n.256T>C (INS-IGF2)
NM_001042376.3:c.197T>C (INS-IGF2)	NP_001035835.1:p.Leu66Ser
NR_003512.4:n.256T>C (INS-IGF2)
NM_001007139.6:c.-459T>C (IGF2)	NP_001007140.2:n.-459T>C