Canonical Allele Identifier: CA1948025701
Gene: INS-IGF2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2159725C= , CM000673.2:g.2159725C= GRCh38
NC_000011.9:g.2180955C= , CM000673.1:g.2180955C= GRCh37
NC_000011.8:g.2137531C= NCBI36
NG_007114.1:g.6470G=
NG_050578.1:g.6485G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356578.8:c.187+1060G= ENSP00000348986.4:n.187+1060G=
ENST00000397270.1:c.187+1060G= ENSP00000380440.1:n.187+1060G=
NM_001042376.2:c.187+1060G= NP_001035835.1:n.187+1060G=
NR_003512.3:n.246+1060G=
NM_001042376.3:c.187+1060G= NP_001035835.1:n.187+1060G=
NR_003512.4:n.246+1060G=
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