Canonical Allele Identifier: CA16606872
Gene: IGF1R HGNC NCBI

Linked Data

ClinVar Variation Id: 392286
ClinVar RCV Id: RCV000439164
dbSNP Id: rs1057524426
MyVariant Identifiers: chr15:g.99456272G>C (hg19) chr15:g.98913043G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.98913043G>C , CM000677.2:g.98913043G>C GRCh38
NC_000015.9:g.99456272G>C , CM000677.1:g.99456272G>C GRCh37
NC_000015.8:g.97273795G>C NCBI36
NG_009492.1:g.268512G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000649865.1:c.1590-1G>C ENSP00000496919.1:n.1590-1G>C
ENST00000650285.1:c.1590-1G>C MANE Select ENSP00000497069.1:n.1590-1G>C
ENST00000268035.10:c.1590-1G>C ENSP00000268035.6:n.1590-1G>C
ENST00000558762.5:c.1590-1G>C ENSP00000453007.1:n.1590-1G>C
ENST00000559582.1:n.497-1G>C
ENST00000559925.5:n.1590-1G>C
NM_000875.4:c.1590-1G>C NP_000866.1:n.1590-1G>C
NM_001291858.1:c.1590-1G>C NP_001278787.1:n.1590-1G>C
XM_011521513.1:c.1653-1G>C XP_011519815.1:n.1653-1G>C
XM_011521514.1:c.1653-1G>C XP_011519816.1:n.1653-1G>C
XM_011521515.1:c.1653-1G>C XP_011519817.1:n.1653-1G>C
XM_011521516.1:c.681-1G>C XP_011519818.1:n.681-1G>C
XM_011521517.1:c.255-1G>C XP_011519819.1:n.255-1G>C
XM_011521516.2:c.681-1G>C XP_011519818.1:n.681-1G>C
XM_011521517.2:c.255-1G>C XP_011519819.1:n.255-1G>C
XM_017022136.1:c.1665-1G>C XP_016877625.1:n.1665-1G>C
XM_017022137.1:c.1665-1G>C XP_016877626.1:n.1665-1G>C
XM_017022138.1:c.1665-1G>C XP_016877627.1:n.1665-1G>C
XM_017022139.1:c.1227-1G>C XP_016877628.1:n.1227-1G>C
XM_024449913.1:c.681-1G>C XP_024305681.1:n.681-1G>C
NM_000875.5:c.1590-1G>C MANE Select NP_000866.1:n.1590-1G>C
NM_001291858.2:c.1590-1G>C NP_001278787.1:n.1590-1G>C
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