Canonical Allele Identifier: CA472029386

Gene: IGF2 INS-IGF2

Linked Data

• gnomAD v4: 11-2149272-A-G
• MyVariant Identifiers: chr11:g.2170502A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2149272A>G , CM000673.2:g.2149272A>G	GRCh38
NC_000011.9:g.2170502A>G , CM000673.1:g.2170502A>G	GRCh37
NC_000011.8:g.2127078A>G	NCBI36
NG_008849.1:g.5332T>C
NG_050578.1:g.16938T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481781.3:c.-395T>C (IGF2)	ENSP00000511998.1:n.-395T>C
ENST00000643349.2:c.108T>C	ENSP00000495715.1:p.Pro36=
ENST00000695541.1:c.-395T>C (IGF2)	ENSP00000511997.1:n.-395T>C
ENST00000481781.2:n.199T>C
ENST00000643349.1:c.108T>C	ENSP00000495715.1:p.Pro36=
ENST00000356578.8:c.261T>C (INS-IGF2)	ENSP00000348986.4:p.Pro87=
ENST00000397270.1:c.261T>C (INS-IGF2)	ENSP00000380440.1:p.Pro87=
ENST00000476874.1:n.144T>C (INS-IGF2)
ENST00000481781.1:n.466T>C (INS-IGF2)
NM_001007139.5:c.-395T>C (IGF2)	NP_001007140.2:n.-395T>C
NM_001042376.2:c.261T>C (INS-IGF2)	NP_001035835.1:p.Pro87=
NR_003512.3:n.320T>C (INS-IGF2)
NM_001042376.3:c.261T>C (INS-IGF2)	NP_001035835.1:p.Pro87=
NR_003512.4:n.320T>C (INS-IGF2)
NM_001007139.6:c.-395T>C (IGF2)	NP_001007140.2:n.-395T>C