Linked Data
ClinVar Variation Id:
305196
dbSNP Id:
rs146630228
ExAC:
11:6412125 C / G
gnomAD v2:
11-6412125-C-G
gnomAD v3:
11-6390895-C-G
gnomAD v4:
11-6390895-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.6390895C>G , CM000673.2:g.6390895C>G | GRCh38 |
| NC_000011.9:g.6412125C>G , CM000673.1:g.6412125C>G | GRCh37 |
| NC_000011.8:g.6368701C>G | NCBI36 |
| NG_011780.1:g.5471C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342245.9:c.297C>G MANE Select | ENSP00000340409.4:p.Thr99= | |
| ENST00000342245.8:c.297C>G | ENSP00000340409.4:p.Thr99= | |
| ENST00000527275.5:c.297C>G | ENSP00000435350.1:p.Thr99= | |
| ENST00000530395.1:c.-96+256C>G | ENSP00000431479.1:n.-96+256C>G | |
| ENST00000531303.5:c.297C>G | ENSP00000432625.1:p.Thr99= | |
| ENST00000533123.5:c.297C>G | ENSP00000435950.1:p.Thr99= | |
| ENST00000533196.1:n.374+82C>G | ||
| ENST00000534405.5:c.297C>G | ENSP00000434353.1:p.Thr99= | |
| NM_000543.4:c.297C>G | NP_000534.3:p.Thr99= | |
| NM_001007593.2:c.297C>G | NP_001007594.2:p.Thr99= | |
| XM_005253075.3:c.297C>G | XP_005253132.1:p.Thr99= | |
| XM_011520303.1:c.297C>G | XP_011518605.1:p.Thr99= | |
| XM_011520304.1:c.297C>G | XP_011518606.1:p.Thr99= | |
| XR_930886.1:n.595C>G | ||
| NM_001318087.1:c.297C>G | NP_001305016.1:p.Thr99= | |
| NM_001318088.1:c.-665C>G | NP_001305017.1:n.-665C>G | |
| NM_001365135.1:c.297C>G | NP_001352064.1:p.Thr99= | |
| NR_027400.2:n.482C>G | ||
| NR_134502.1:n.482C>G | ||
| XM_011520304.2:c.297C>G | XP_011518606.1:p.Thr99= | |
| XR_001747940.2:n.422C>G | ||
| XR_002957158.1:n.422C>G | ||
| NM_000543.5:c.297C>G MANE Select | NP_000534.3:p.Thr99= | |
| NM_001007593.3:c.297C>G | NP_001007594.2:p.Thr99= | |
| NM_001318087.2:c.297C>G | NP_001305016.1:p.Thr99= | |
| NM_001318088.2:c.-665C>G | NP_001305017.1:n.-665C>G | |
| NM_001365135.2:c.297C>G | NP_001352064.1:p.Thr99= | |
| NR_027400.3:n.422C>G | ||
| NR_134502.2:n.422C>G |