Canonical Allele Identifier: CA674546614

Gene: IGF2 INS-IGF2

Linked Data

• dbSNP Id: rs1242145346
• MyVariant Identifiers: chr11:g.2170117C>T (hg19) ; chr11:g.2148887C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2148887C>T , CM000673.2:g.2148887C>T	GRCh38
NC_000011.9:g.2170117C>T , CM000673.1:g.2170117C>T	GRCh37
NC_000011.8:g.2126693C>T	NCBI36
NG_008849.1:g.5717G>A
NG_050578.1:g.17323G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000481781.3:c.-249+239G>A (IGF2)	ENSP00000511998.1:n.-249+239G>A
ENST00000643349.2:c.254+239G>A	ENSP00000495715.1:n.254+239G>A
ENST00000695541.1:c.-249+239G>A (IGF2)	ENSP00000511997.1:n.-249+239G>A
ENST00000481781.2:n.345+239G>A
ENST00000643349.1:c.254+239G>A	ENSP00000495715.1:n.254+239G>A
ENST00000356578.8:c.407+239G>A (INS-IGF2)	ENSP00000348986.4:n.407+239G>A
ENST00000397270.1:c.407+239G>A (INS-IGF2)	ENSP00000380440.1:n.407+239G>A
ENST00000481781.1:n.612+239G>A (INS-IGF2)
NM_001007139.5:c.-249+239G>A (IGF2)	NP_001007140.2:n.-249+239G>A
NM_001042376.2:c.407+239G>A (INS-IGF2)	NP_001035835.1:n.407+239G>A
NR_003512.3:n.466+239G>A (INS-IGF2)
NM_001042376.3:c.407+239G>A (INS-IGF2)	NP_001035835.1:n.407+239G>A
NR_003512.4:n.466+239G>A (INS-IGF2)
NM_001007139.6:c.-249+239G>A (IGF2)	NP_001007140.2:n.-249+239G>A