Canonical Allele Identifier: CA472027780

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2148544A>T , CM000673.2:g.2148544A>T GRCh38
NC_000011.9:g.2169774A>T , CM000673.1:g.2169774A>T GRCh37
NC_000011.8:g.2126350A>T NCBI36
NG_008849.1:g.6060T>A
NG_050578.1:g.17666T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000481781.3:c.-249+582T>A (IGF2) ENSP00000511998.1:n.-249+582T>A
ENST00000643349.2:c.254+582T>A ENSP00000495715.1:n.254+582T>A
ENST00000695541.1:c.-249+582T>A (IGF2) ENSP00000511997.1:n.-249+582T>A
ENST00000481781.2:n.345+582T>A
ENST00000643349.1:c.254+582T>A ENSP00000495715.1:n.254+582T>A
ENST00000356578.8:c.407+582T>A (INS-IGF2) ENSP00000348986.4:n.407+582T>A
ENST00000397270.1:c.407+582T>A (INS-IGF2) ENSP00000380440.1:n.407+582T>A
ENST00000481781.1:n.612+582T>A (INS-IGF2)
NM_001007139.5:c.-249+582T>A (IGF2) NP_001007140.2:n.-249+582T>A
NM_001042376.2:c.407+582T>A (INS-IGF2) NP_001035835.1:n.407+582T>A
NR_003512.3:n.466+582T>A (INS-IGF2)
NR_028043.2:n.1946A>T (IGF2-AS)
NR_133657.1:n.1835A>T (IGF2-AS)
NM_001042376.3:c.407+582T>A (INS-IGF2) NP_001035835.1:n.407+582T>A
NR_003512.4:n.466+582T>A (INS-IGF2)
NM_001007139.6:c.-249+582T>A (IGF2) NP_001007140.2:n.-249+582T>A