Canonical Allele Identifier: CA379118123

Gene: IGF2 INS-IGF2

Linked Data

• MyVariant Identifiers: chr11:g.2170392G>C (hg19) ; chr11:g.2149162G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2149162G>C , CM000673.2:g.2149162G>C	GRCh38
NC_000011.9:g.2170392G>C , CM000673.1:g.2170392G>C	GRCh37
NC_000011.8:g.2126968G>C	NCBI36
NG_008849.1:g.5442C>G
NG_050578.1:g.17048C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481781.3:c.-285C>G (IGF2)	ENSP00000511998.1:n.-285C>G
ENST00000643349.2:c.218C>G	ENSP00000495715.1:p.Pro73Arg
ENST00000695541.1:c.-285C>G (IGF2)	ENSP00000511997.1:n.-285C>G
ENST00000481781.2:n.309C>G
ENST00000643349.1:c.218C>G	ENSP00000495715.1:p.Pro73Arg
ENST00000356578.8:c.371C>G (INS-IGF2)	ENSP00000348986.4:p.Pro124Arg
ENST00000397270.1:c.371C>G (INS-IGF2)	ENSP00000380440.1:p.Pro124Arg
ENST00000476874.1:n.254C>G (INS-IGF2)
ENST00000481781.1:n.576C>G (INS-IGF2)
NM_001007139.5:c.-285C>G (IGF2)	NP_001007140.2:n.-285C>G
NM_001042376.2:c.371C>G (INS-IGF2)	NP_001035835.1:p.Pro124Arg
NR_003512.3:n.430C>G (INS-IGF2)
NM_001042376.3:c.371C>G (INS-IGF2)	NP_001035835.1:p.Pro124Arg
NR_003512.4:n.430C>G (INS-IGF2)
NM_001007139.6:c.-285C>G (IGF2)	NP_001007140.2:n.-285C>G