Canonical Allele Identifier: CA379118642

Gene: IGF2 INS-IGF2

Linked Data

• dbSNP Id: rs759261999
• gnomAD v3: 11-2149300-C-T
• gnomAD v4: 11-2149300-C-T
• MyVariant Identifiers: chr11:g.2170530C>T (hg19) ; chr11:g.2149300C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2149300C>T , CM000673.2:g.2149300C>T	GRCh38
NC_000011.9:g.2170530C>T , CM000673.1:g.2170530C>T	GRCh37
NC_000011.8:g.2127106C>T	NCBI36
NG_008849.1:g.5304G>A
NG_050578.1:g.16910G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481781.3:c.-423G>A (IGF2)	ENSP00000511998.1:n.-423G>A
ENST00000643349.2:c.80G>A	ENSP00000495715.1:p.Gly27Asp
ENST00000695541.1:c.-423G>A (IGF2)	ENSP00000511997.1:n.-423G>A
ENST00000481781.2:n.171G>A
ENST00000643349.1:c.80G>A	ENSP00000495715.1:p.Gly27Asp
ENST00000356578.8:c.233G>A (INS-IGF2)	ENSP00000348986.4:p.Gly78Asp
ENST00000397270.1:c.233G>A (INS-IGF2)	ENSP00000380440.1:p.Gly78Asp
ENST00000476874.1:n.116G>A (INS-IGF2)
ENST00000481781.1:n.438G>A (INS-IGF2)
NM_001007139.5:c.-423G>A (IGF2)	NP_001007140.2:n.-423G>A
NM_001042376.2:c.233G>A (INS-IGF2)	NP_001035835.1:p.Gly78Asp
NR_003512.3:n.292G>A (INS-IGF2)
NM_001042376.3:c.233G>A (INS-IGF2)	NP_001035835.1:p.Gly78Asp
NR_003512.4:n.292G>A (INS-IGF2)
NM_001007139.6:c.-423G>A (IGF2)	NP_001007140.2:n.-423G>A