Linked Data
ClinVar Variation Id:
1786277
ClinVar RCV Id:
RCV002417654
dbSNP Id:
rs769375972
ExAC:
7:117232344 T / C
gnomAD v2:
7-117232344-T-C
gnomAD v3:
7-117592290-T-C
gnomAD v4:
7-117592290-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.117592290T>C , CM000669.2:g.117592290T>C | GRCh38 |
| NC_000007.13:g.117232344T>C , CM000669.1:g.117232344T>C | GRCh37 |
| NC_000007.12:g.117019580T>C | NCBI36 |
| NG_016465.4:g.131507T>C , LRG_663:g.131507T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000647720.2:c.2123T>C | ENSP00000497673.2:p.Ile708Thr | |
| ENST00000647978.2:c.*1837T>C | ENSP00000497658.1:n.*1837T>C | |
| ENST00000649781.2:c.1940T>C | ENSP00000497203.1:p.Ile647Thr | |
| ENST00000685018.2:c.2123T>C | ENSP00000510194.2:p.Ile708Thr | |
| ENST00000687278.2:c.2123T>C | ENSP00000509593.2:p.Ile708Thr | |
| ENST00000699585.1:c.2123T>C | ENSP00000514456.1:p.Ile708Thr | |
| ENST00000699598.1:c.2123T>C | ENSP00000514467.1:p.Ile708Thr | |
| ENST00000699599.1:c.2123T>C | ENSP00000514468.1:p.Ile708Thr | |
| ENST00000699600.1:c.2123T>C | ENSP00000514469.1:p.Ile708Thr | |
| ENST00000699601.1:c.*423T>C | ENSP00000514470.1:n.*423T>C | |
| ENST00000699602.1:c.2123T>C | ENSP00000514471.1:p.Ile708Thr | |
| ENST00000699604.1:c.*1947T>C | ENSP00000514472.1:n.*1947T>C | |
| ENST00000699605.1:c.1697T>C | ENSP00000514473.1:p.Ile566Thr | |
| ENST00000003084.11:c.2123T>C MANE Select | ENSP00000003084.6:p.Ile708Thr | |
| ENST00000647978.1:c.*1837T>C | ENSP00000497658.1:n.*1837T>C | |
| ENST00000648260.1:c.1402-10536T>C | ENSP00000497957.1:n.1402-10536T>C | |
| ENST00000649406.1:c.1940T>C | ENSP00000497965.1:p.Ile647Thr | |
| ENST00000649781.1:c.1940T>C | ENSP00000497203.1:p.Ile647Thr | |
| ENST00000003084.10:c.2123T>C | ENSP00000003084.6:p.Ile708Thr | |
| ENST00000426809.5:c.2033T>C | ENSP00000389119.1:p.Ile678Thr | |
| NM_000492.3:c.2123T>C , LRG_663t1:c.2123T>C | NP_000483.3:p.Ile708Thr | |
| XM_011515751.1:c.2213T>C | XP_011514053.1:p.Ile738Thr | |
| XM_011515752.1:c.2213T>C | XP_011514054.1:p.Ile738Thr | |
| XM_011515753.1:c.1880T>C | XP_011514055.1:p.Ile627Thr | |
| XM_011515754.1:c.1880T>C | XP_011514056.1:p.Ile627Thr | |
| NM_000492.4:c.2123T>C MANE Select | NP_000483.3:p.Ile708Thr |