gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.72419628 (AMR)
Genomes Max Group AF
0.72419628 (AMR)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.102400737G>A , CM000674.2:g.102400737G>A | GRCh38 |
| NC_000012.11:g.102794515G>A , CM000674.1:g.102794515G>A | GRCh37 |
| NC_000012.10:g.101318645G>A | NCBI36 |
| NG_011713.1:g.84864C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000337514.11:c.*1770C>T (IGF1) MANE Select | ENSP00000337612.7:n.*1770C>T | |
| ENST00000337514.10:c.*1770C>T (IGF1) | ENSP00000337612.6:n.*1770C>T | |
| ENST00000456098.5:c.*1804C>T (IGF1) | ENSP00000394999.1:n.*1804C>T | |
| NM_000618.3:c.*1770C>T (IGF1) | NP_000609.1:n.*1770C>T | |
| NM_000618.4:c.*1770C>T (IGF1) | NP_000609.1:n.*1770C>T | |
| NM_001111283.1:c.*1804C>T (IGF1) | NP_001104753.1:n.*1804C>T | |
| NM_001111283.2:c.*1804C>T (IGF1) | NP_001104753.1:n.*1804C>T | |
| NM_001111284.1:c.*1770C>T (IGF1) | NP_001104754.1:n.*1770C>T | |
| XR_944534.1:n.4791C>T (IGF1) | ||
| XR_944535.1:n.4568C>T (IGF1) | ||
| XR_944536.1:n.4553C>T (IGF1) | ||
| XR_945270.1:n.582-3376G>A (LINC02456) | ||
| XR_945271.1:n.582-3376G>A (LINC02456) | ||
| XR_945272.1:n.582-3376G>A (LINC02456) | ||
| XR_945273.1:n.532-3376G>A (LINC02456) | ||
| XR_945274.1:n.258-3376G>A (LINC02456) | ||
| XR_945275.1:n.138-3376G>A (LINC02456) | ||
| XR_945276.1:n.110-3376G>A (LINC02456) | ||
| XR_945277.1:n.582-3376G>A (LINC02456) | ||
| XM_017019262.2:c.*1804C>T (IGF1) | XP_016874751.1:n.*1804C>T | |
| XM_017019263.2:c.*1770C>T (IGF1) | XP_016874752.1:n.*1770C>T | |
| XR_001749285.1:n.697-3376G>A (LINC02456) | ||
| XR_001749286.1:n.258-3376G>A (LINC02456) | ||
| XR_001749287.1:n.576-3376G>A (LINC02456) | ||
| XR_001749288.1:n.1585-3376G>A (LINC02456) | ||
| NM_000618.5:c.*1770C>T (IGF1) MANE Select | NP_000609.1:n.*1770C>T | |
| NM_001111283.3:c.*1804C>T (IGF1) | NP_001104753.1:n.*1804C>T | |
| NM_001111284.2:c.*1770C>T (IGF1) | NP_001104754.1:n.*1770C>T |