Canonical Allele Identifier: CA216261941

Gene: IGF2 INS-IGF2 IGF2-AS

Linked Data

• dbSNP Id: rs1036174346
• gnomAD v4: 11-2148636-T-C
• MyVariant Identifiers: chr11:g.2169866T>C (hg19) ; chr11:g.2148636T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2148636T>C , CM000673.2:g.2148636T>C	GRCh38
NC_000011.9:g.2169866T>C , CM000673.1:g.2169866T>C	GRCh37
NC_000011.8:g.2126442T>C	NCBI36
NG_008849.1:g.5968A>G
NG_050578.1:g.17574A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481781.3:c.-249+490A>G (IGF2)	ENSP00000511998.1:n.-249+490A>G
ENST00000643349.2:c.254+490A>G	ENSP00000495715.1:n.254+490A>G
ENST00000695541.1:c.-249+490A>G (IGF2)	ENSP00000511997.1:n.-249+490A>G
ENST00000481781.2:n.345+490A>G
ENST00000643349.1:c.254+490A>G	ENSP00000495715.1:n.254+490A>G
ENST00000356578.8:c.407+490A>G (INS-IGF2)	ENSP00000348986.4:n.407+490A>G
ENST00000397270.1:c.407+490A>G (INS-IGF2)	ENSP00000380440.1:n.407+490A>G
ENST00000481781.1:n.612+490A>G (INS-IGF2)
NM_001007139.5:c.-249+490A>G (IGF2)	NP_001007140.2:n.-249+490A>G
NM_001042376.2:c.407+490A>G (INS-IGF2)	NP_001035835.1:n.407+490A>G
NR_003512.3:n.466+490A>G (INS-IGF2)
NR_028043.2:n.2038T>C (IGF2-AS)
NR_133657.1:n.1927T>C (IGF2-AS)
NM_001042376.3:c.407+490A>G (INS-IGF2)	NP_001035835.1:n.407+490A>G
NR_003512.4:n.466+490A>G (INS-IGF2)
NM_001007139.6:c.-249+490A>G (IGF2)	NP_001007140.2:n.-249+490A>G