Canonical Allele Identifier: CA379118671

Gene: IGF2 INS-IGF2

Linked Data

• MyVariant Identifiers: chr11:g.2170537G>A (hg19) ; chr11:g.2149307G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2149307G>A , CM000673.2:g.2149307G>A	GRCh38
NC_000011.9:g.2170537G>A , CM000673.1:g.2170537G>A	GRCh37
NC_000011.8:g.2127113G>A	NCBI36
NG_008849.1:g.5297C>T
NG_050578.1:g.16903C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481781.3:c.-430C>T (IGF2)	ENSP00000511998.1:n.-430C>T
ENST00000643349.2:c.73C>T	ENSP00000495715.1:p.Pro25Ser
ENST00000695541.1:c.-430C>T (IGF2)	ENSP00000511997.1:n.-430C>T
ENST00000481781.2:n.164C>T
ENST00000643349.1:c.73C>T	ENSP00000495715.1:p.Pro25Ser
ENST00000356578.8:c.226C>T (INS-IGF2)	ENSP00000348986.4:p.Pro76Ser
ENST00000397270.1:c.226C>T (INS-IGF2)	ENSP00000380440.1:p.Pro76Ser
ENST00000476874.1:n.109C>T (INS-IGF2)
ENST00000481781.1:n.431C>T (INS-IGF2)
NM_001007139.5:c.-430C>T (IGF2)	NP_001007140.2:n.-430C>T
NM_001042376.2:c.226C>T (INS-IGF2)	NP_001035835.1:p.Pro76Ser
NR_003512.3:n.285C>T (INS-IGF2)
NM_001042376.3:c.226C>T (INS-IGF2)	NP_001035835.1:p.Pro76Ser
NR_003512.4:n.285C>T (INS-IGF2)
NM_001007139.6:c.-430C>T (IGF2)	NP_001007140.2:n.-430C>T