Linked Data
ClinVar Variation Id:
566403
ClinVar RCV Id:
RCV000686205
dbSNP Id:
rs750671325
ExAC:
2:217280203 T / C
gnomAD v2:
2-217280203-T-C
gnomAD v4:
2-216415480-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.216415480T>C , CM000664.2:g.216415480T>C | GRCh38 |
| NC_000002.11:g.217280203T>C , CM000664.1:g.217280203T>C | GRCh37 |
| NC_000002.10:g.216988448T>C | NCBI36 |
| NG_009771.1:g.8067T>C , LRG_108:g.8067T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000425815.6:c.776T>C | ENSP00000394410.2:p.Ile259Thr | |
| ENST00000430374.6:c.776T>C | ENSP00000405077.2:p.Ile259Thr | |
| ENST00000444508.6:c.776T>C | ENSP00000398969.2:p.Ile259Thr | |
| ENST00000697898.1:n.1137T>C | ||
| ENST00000697899.1:c.776T>C | ENSP00000513470.1:p.Ile259Thr | |
| ENST00000697900.1:n.1052T>C | ||
| ENST00000697901.1:c.776T>C | ENSP00000513471.1:p.Ile259Thr | |
| ENST00000697902.1:n.1008T>C | ||
| ENST00000697903.1:c.776T>C | ENSP00000513472.1:p.Ile259Thr | |
| ENST00000697904.1:c.776T>C | ENSP00000513473.1:p.Ile259Thr | |
| ENST00000697905.1:c.776T>C | ENSP00000513474.1:p.Ile259Thr | |
| ENST00000697906.1:c.776T>C | ENSP00000513475.1:p.Ile259Thr | |
| ENST00000697907.1:c.776T>C | ENSP00000513476.1:p.Ile259Thr | |
| ENST00000357276.9:c.776T>C MANE Select | ENSP00000349823.4:p.Ile259Thr | |
| ENST00000357276.8:c.776T>C | ENSP00000349823.4:p.Ile259Thr | |
| ENST00000358207.9:c.776T>C | ENSP00000350940.5:p.Ile259Thr | |
| ENST00000392128.6:c.368T>C | ENSP00000375974.2:p.Ile123Thr | |
| ENST00000427645.5:c.473T>C | ENSP00000392997.1:p.Ile158Thr | |
| NM_001127207.1:c.776T>C | NP_001120679.1:p.Ile259Thr | |
| NM_014140.3:c.776T>C , LRG_108t1:c.776T>C | NP_054859.2:p.Ile259Thr | |
| XM_005246631.2:c.776T>C | XP_005246688.1:p.Ile259Thr | |
| XM_005246632.1:c.776T>C | XP_005246689.1:p.Ile259Thr | |
| XM_006712557.1:c.776T>C | XP_006712620.1:p.Ile259Thr | |
| XM_005246632.2:c.776T>C | XP_005246689.1:p.Ile259Thr | |
| XM_017004228.2:c.-141T>C | XP_016859717.1:n.-141T>C | |
| NM_001127207.2:c.776T>C | NP_001120679.1:p.Ile259Thr | |
| NM_014140.4:c.776T>C MANE Select | NP_054859.2:p.Ile259Thr |