Linked Data
ClinVar Variation Id:
1150073
ClinVar RCV Id:
RCV001490526
dbSNP Id:
rs536760557
gnomAD v2:
11-6413192-C-T
gnomAD v3:
11-6391962-C-T
gnomAD v4:
11-6391962-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.6391962C>T , CM000673.2:g.6391962C>T | GRCh38 |
| NC_000011.9:g.6413192C>T , CM000673.1:g.6413192C>T | GRCh37 |
| NC_000011.8:g.6369768C>T | NCBI36 |
| NG_011780.1:g.6538C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000342245.9:c.897C>T MANE Select | ENSP00000340409.4:p.Thr299= | |
| ENST00000342245.8:c.897C>T | ENSP00000340409.4:p.Thr299= | |
| ENST00000526280.1:c.86C>T | ||
| ENST00000527275.5:c.894C>T | ENSP00000435350.1:p.Thr298= | |
| ENST00000530395.1:c.78C>T | ENSP00000431479.1:p.Thr26= | |
| ENST00000531303.5:c.438+459C>T | ENSP00000432625.1:n.438+459C>T | |
| ENST00000533123.5:c.897C>T | ENSP00000435950.1:p.Thr299= | |
| ENST00000533196.1:n.375-44C>T | ||
| ENST00000534405.5:c.897C>T | ENSP00000434353.1:p.Thr299= | |
| NM_000543.4:c.897C>T | NP_000534.3:p.Thr299= | |
| NM_001007593.2:c.894C>T | NP_001007594.2:p.Thr298= | |
| XM_005253075.3:c.897C>T | XP_005253132.1:p.Thr299= | |
| XM_011520303.1:c.897C>T | XP_011518605.1:p.Thr299= | |
| XM_011520304.1:c.897C>T | XP_011518606.1:p.Thr299= | |
| XR_930886.1:n.1195C>T | ||
| NM_001318087.1:c.897C>T | NP_001305016.1:p.Thr299= | |
| NM_001318088.1:c.-65C>T | NP_001305017.1:n.-65C>T | |
| NM_001365135.1:c.897C>T | NP_001352064.1:p.Thr299= | |
| NR_027400.2:n.1082C>T | ||
| NR_134502.1:n.623+459C>T | ||
| XM_011520304.2:c.897C>T | XP_011518606.1:p.Thr299= | |
| XR_001747940.2:n.1022C>T | ||
| XR_002957158.1:n.1022C>T | ||
| NM_000543.5:c.897C>T MANE Select | NP_000534.3:p.Thr299= | |
| NM_001007593.3:c.894C>T | NP_001007594.2:p.Thr298= | |
| NM_001318087.2:c.897C>T | NP_001305016.1:p.Thr299= | |
| NM_001318088.2:c.-65C>T | NP_001305017.1:n.-65C>T | |
| NM_001365135.2:c.897C>T | NP_001352064.1:p.Thr299= | |
| NR_027400.3:n.1022C>T | ||
| NR_134502.2:n.563+459C>T |