Linked Data
ClinVar Variation Id:
289679
dbSNP Id:
rs778474394
ExAC:
2:238253293 C / T
gnomAD v2:
2-238253293-C-T
gnomAD v3:
2-237344650-C-T
gnomAD v4:
2-237344650-C-T
COSMIC:
COSM6090910
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.237344650C>T , CM000664.2:g.237344650C>T | GRCh38 |
| NC_000002.11:g.238253293C>T , CM000664.1:g.238253293C>T | GRCh37 |
| NC_000002.10:g.237918032C>T | NCBI36 |
| NG_008676.1:g.74558G>A , LRG_473:g.74558G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000347401.8:c.13G>A | ||
| ENST00000353578.9:c.6750G>A | ENSP00000315873.4:p.Thr2250= | |
| ENST00000295550.9:c.7368G>A MANE Select | ENSP00000295550.4:p.Thr2456= | |
| ENST00000295550.8:c.7368G>A | ENSP00000295550.4:p.Thr2456= | |
| ENST00000347401.7:c.5544G>A | ENSP00000315609.4:p.Thr1848= | |
| ENST00000353578.8:c.6750G>A | ENSP00000315873.4:p.Thr2250= | |
| ENST00000409809.5:c.6750G>A | ENSP00000386844.1:p.Thr2250= | |
| ENST00000472056.5:c.5547G>A | ENSP00000418285.1:p.Thr1849= | |
| ENST00000491769.1:n.1622G>A | ||
| NM_004369.3:c.7368G>A , LRG_473t1:c.7368G>A | NP_004360.2:p.Thr2456= | |
| NM_057166.4:c.5547G>A | NP_476507.3:p.Thr1849= | |
| NM_057167.3:c.6750G>A | NP_476508.2:p.Thr2250= | |
| XM_005246065.1:c.6768G>A | XP_005246122.1:p.Thr2256= | |
| XM_005246066.1:c.6147G>A | XP_005246123.1:p.Thr2049= | |
| XM_006712253.1:c.6867G>A | XP_006712316.1:p.Thr2289= | |
| XM_011510574.1:c.7365G>A | XP_011508876.1:p.Thr2455= | |
| XM_011510575.1:c.4962G>A | XP_011508877.1:p.Thr1654= | |
| XM_017003304.1:c.4962G>A | XP_016858793.1:p.Thr1654= | |
| XM_024452684.1:c.6147G>A | XP_024308452.1:p.Thr2049= | |
| NM_004369.4:c.7368G>A MANE Select | NP_004360.2:p.Thr2456= | |
| NM_057166.5:c.5547G>A | NP_476507.3:p.Thr1849= | |
| NM_057167.4:c.6750G>A | NP_476508.2:p.Thr2250= |