Canonical Allele Identifier: CA472029347

Gene: IGF2 INS-IGF2

Linked Data

• dbSNP Id: rs1289769753
• gnomAD v2: 11-2170487-A-T
• gnomAD v3: 11-2149257-A-T
• gnomAD v4: 11-2149257-A-T
• MyVariant Identifiers: chr11:g.2170487A>T (hg19) ; chr11:g.2149257A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2149257A>T , CM000673.2:g.2149257A>T	GRCh38
NC_000011.9:g.2170487A>T , CM000673.1:g.2170487A>T	GRCh37
NC_000011.8:g.2127063A>T	NCBI36
NG_008849.1:g.5347T>A
NG_050578.1:g.16953T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481781.3:c.-380T>A (IGF2)	ENSP00000511998.1:n.-380T>A
ENST00000643349.2:c.123T>A	ENSP00000495715.1:p.Thr41=
ENST00000695541.1:c.-380T>A (IGF2)	ENSP00000511997.1:n.-380T>A
ENST00000481781.2:n.214T>A
ENST00000643349.1:c.123T>A	ENSP00000495715.1:p.Thr41=
ENST00000356578.8:c.276T>A (INS-IGF2)	ENSP00000348986.4:p.Thr92=
ENST00000397270.1:c.276T>A (INS-IGF2)	ENSP00000380440.1:p.Thr92=
ENST00000476874.1:n.159T>A (INS-IGF2)
ENST00000481781.1:n.481T>A (INS-IGF2)
NM_001007139.5:c.-380T>A (IGF2)	NP_001007140.2:n.-380T>A
NM_001042376.2:c.276T>A (INS-IGF2)	NP_001035835.1:p.Thr92=
NR_003512.3:n.335T>A (INS-IGF2)
NM_001042376.3:c.276T>A (INS-IGF2)	NP_001035835.1:p.Thr92=
NR_003512.4:n.335T>A (INS-IGF2)
NM_001007139.6:c.-380T>A (IGF2)	NP_001007140.2:n.-380T>A