Canonical Allele Identifier: CA5818025
Gene: IGF2 HGNC NCBI
INS-IGF2 HGNC NCBI

Linked Data

dbSNP Id: rs779818488
gnomAD v2: 11-2170393-G-A
gnomAD v4: 11-2149163-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2149163G>A , CM000673.2:g.2149163G>A GRCh38
NC_000011.9:g.2170393G>A , CM000673.1:g.2170393G>A GRCh37
NC_000011.8:g.2126969G>A NCBI36
NG_008849.1:g.5441C>T
NG_050578.1:g.17047C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000481781.3:c.-286C>T (IGF2) ENSP00000511998.1:n.-286C>T
ENST00000643349.2:c.217C>T ENSP00000495715.1:p.Pro73Ser
ENST00000695541.1:c.-286C>T (IGF2) ENSP00000511997.1:n.-286C>T
ENST00000481781.2:n.308C>T
ENST00000643349.1:c.217C>T ENSP00000495715.1:p.Pro73Ser
ENST00000356578.8:c.370C>T (INS-IGF2) ENSP00000348986.4:p.Pro124Ser
ENST00000397270.1:c.370C>T (INS-IGF2) ENSP00000380440.1:p.Pro124Ser
ENST00000476874.1:n.253C>T (INS-IGF2)
ENST00000481781.1:n.575C>T (INS-IGF2)
NM_001007139.5:c.-286C>T (IGF2) NP_001007140.2:n.-286C>T
NM_001042376.2:c.370C>T (INS-IGF2) NP_001035835.1:p.Pro124Ser
NR_003512.3:n.429C>T (INS-IGF2)
NM_001042376.3:c.370C>T (INS-IGF2) NP_001035835.1:p.Pro124Ser
NR_003512.4:n.429C>T (INS-IGF2)
NM_001007139.6:c.-286C>T (IGF2) NP_001007140.2:n.-286C>T