Canonical Allele Identifier: CA216262410

Gene: IGF2 INS-IGF2

Linked Data

• dbSNP Id: rs905672114
• MyVariant Identifiers: chr11:g.2170493C>A (hg19) ; chr11:g.2149263C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2149263C>A , CM000673.2:g.2149263C>A	GRCh38
NC_000011.9:g.2170493C>A , CM000673.1:g.2170493C>A	GRCh37
NC_000011.8:g.2127069C>A	NCBI36
NG_008849.1:g.5341G>T
NG_050578.1:g.16947G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481781.3:c.-386G>T (IGF2)	ENSP00000511998.1:n.-386G>T
ENST00000643349.2:c.117G>T	ENSP00000495715.1:p.Val39=
ENST00000695541.1:c.-386G>T (IGF2)	ENSP00000511997.1:n.-386G>T
ENST00000481781.2:n.208G>T
ENST00000643349.1:c.117G>T	ENSP00000495715.1:p.Val39=
ENST00000356578.8:c.270G>T (INS-IGF2)	ENSP00000348986.4:p.Val90=
ENST00000397270.1:c.270G>T (INS-IGF2)	ENSP00000380440.1:p.Val90=
ENST00000476874.1:n.153G>T (INS-IGF2)
ENST00000481781.1:n.475G>T (INS-IGF2)
NM_001007139.5:c.-386G>T (IGF2)	NP_001007140.2:n.-386G>T
NM_001042376.2:c.270G>T (INS-IGF2)	NP_001035835.1:p.Val90=
NR_003512.3:n.329G>T (INS-IGF2)
NM_001042376.3:c.270G>T (INS-IGF2)	NP_001035835.1:p.Val90=
NR_003512.4:n.329G>T (INS-IGF2)
NM_001007139.6:c.-386G>T (IGF2)	NP_001007140.2:n.-386G>T