Canonical Allele Identifier: CA472029056

Gene: IGF2 INS-IGF2

Linked Data

• dbSNP Id: rs1425514342
• gnomAD v2: 11-2170391-T-C
• gnomAD v3: 11-2149161-T-C
• gnomAD v4: 11-2149161-T-C
• MyVariant Identifiers: chr11:g.2170391T>C (hg19) ; chr11:g.2149161T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2149161T>C , CM000673.2:g.2149161T>C	GRCh38
NC_000011.9:g.2170391T>C , CM000673.1:g.2170391T>C	GRCh37
NC_000011.8:g.2126967T>C	NCBI36
NG_008849.1:g.5443A>G
NG_050578.1:g.17049A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481781.3:c.-284A>G (IGF2)	ENSP00000511998.1:n.-284A>G
ENST00000643349.2:c.219A>G	ENSP00000495715.1:p.Pro73=
ENST00000695541.1:c.-284A>G (IGF2)	ENSP00000511997.1:n.-284A>G
ENST00000481781.2:n.310A>G
ENST00000643349.1:c.219A>G	ENSP00000495715.1:p.Pro73=
ENST00000356578.8:c.372A>G (INS-IGF2)	ENSP00000348986.4:p.Pro124=
ENST00000397270.1:c.372A>G (INS-IGF2)	ENSP00000380440.1:p.Pro124=
ENST00000476874.1:n.255A>G (INS-IGF2)
ENST00000481781.1:n.577A>G (INS-IGF2)
NM_001007139.5:c.-284A>G (IGF2)	NP_001007140.2:n.-284A>G
NM_001042376.2:c.372A>G (INS-IGF2)	NP_001035835.1:p.Pro124=
NR_003512.3:n.431A>G (INS-IGF2)
NM_001042376.3:c.372A>G (INS-IGF2)	NP_001035835.1:p.Pro124=
NR_003512.4:n.431A>G (INS-IGF2)
NM_001007139.6:c.-284A>G (IGF2)	NP_001007140.2:n.-284A>G