Canonical Allele Identifier: CA472025227

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2147880A>T , CM000673.2:g.2147880A>T GRCh38
NC_000011.9:g.2169110A>T , CM000673.1:g.2169110A>T GRCh37
NC_000011.8:g.2125686A>T NCBI36
NG_008849.1:g.6724T>A
NG_050578.1:g.18330T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000481781.3:c.-248-73T>A (IGF2) ENSP00000511998.1:n.-248-73T>A
ENST00000643349.2:c.255-73T>A ENSP00000495715.1:n.255-73T>A
ENST00000695541.1:c.-248-73T>A (IGF2) ENSP00000511997.1:n.-248-73T>A
ENST00000481781.2:n.346-73T>A
ENST00000643349.1:c.255-73T>A ENSP00000495715.1:n.255-73T>A
ENST00000356578.8:c.408-73T>A (INS-IGF2) ENSP00000348986.4:n.408-73T>A
ENST00000397270.1:c.408-73T>A (INS-IGF2) ENSP00000380440.1:n.408-73T>A
ENST00000481781.1:n.613-73T>A (INS-IGF2)
NM_001007139.5:c.-248-73T>A (IGF2) NP_001007140.2:n.-248-73T>A
NM_001042376.2:c.408-73T>A (INS-IGF2) NP_001035835.1:n.408-73T>A
NR_003512.3:n.467-73T>A (INS-IGF2)
NR_028043.2:n.1282A>T (IGF2-AS)
NR_133657.1:n.1171A>T (IGF2-AS)
NM_001042376.3:c.408-73T>A (INS-IGF2) NP_001035835.1:n.408-73T>A
NR_003512.4:n.467-73T>A (INS-IGF2)
NM_001007139.6:c.-248-73T>A (IGF2) NP_001007140.2:n.-248-73T>A