Canonical Allele Identifier: CA5818000

Linked Data

dbSNP Id: rs10770125
gnomAD v2: 11-2169014-A-G
gnomAD v3: 11-2147784-A-G
gnomAD v4: 11-2147784-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2147784A>G , CM000673.2:g.2147784A>G GRCh38
NC_000011.9:g.2169014A>G , CM000673.1:g.2169014A>G GRCh37
NC_000011.8:g.2125590A>G NCBI36
NG_008849.1:g.6820T>C
NG_050578.1:g.18426T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000481781.3:c.-225T>C (IGF2) ENSP00000511998.1:n.-225T>C
ENST00000643349.2:c.278T>C ENSP00000495715.1:p.Leu93Pro
ENST00000695541.1:c.-225T>C (IGF2) ENSP00000511997.1:n.-225T>C
ENST00000481781.2:n.369T>C
ENST00000643349.1:c.278T>C ENSP00000495715.1:p.Leu93Pro
ENST00000356578.8:c.431T>C (INS-IGF2) ENSP00000348986.4:p.Leu144Pro
ENST00000397270.1:c.431T>C (INS-IGF2) ENSP00000380440.1:p.Leu144Pro
ENST00000481781.1:n.636T>C (INS-IGF2)
NM_001007139.5:c.-225T>C (IGF2) NP_001007140.2:n.-225T>C
NM_001042376.2:c.431T>C (INS-IGF2) NP_001035835.1:p.Leu144Pro
NR_003512.3:n.490T>C (INS-IGF2)
NR_028043.2:n.1186A>G (IGF2-AS)
NR_133657.1:n.1075A>G (IGF2-AS)
NM_001042376.3:c.431T>C (INS-IGF2) NP_001035835.1:p.Leu144Pro
NR_003512.4:n.490T>C (INS-IGF2)
NM_001007139.6:c.-225T>C (IGF2) NP_001007140.2:n.-225T>C