Linked Data
ClinVar Variation Id:
463759
dbSNP Id:
rs1447544874
gnomAD v2:
16-68863642-T-C
gnomAD v4:
16-68829739-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.68829739T>C , CM000678.2:g.68829739T>C | GRCh38 |
| NC_000016.9:g.68863642T>C , CM000678.1:g.68863642T>C | GRCh37 |
| NC_000016.8:g.67421143T>C | NCBI36 |
| NG_008021.1:g.97448T>C , LRG_301:g.97448T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261769.10:c.2381T>C MANE Select | ENSP00000261769.4:p.Val794Ala | |
| ENST00000261769.9:c.2381T>C | ENSP00000261769.4:p.Val794Ala | |
| ENST00000422392.6:c.2198T>C | ENSP00000414946.2:p.Val733Ala | |
| ENST00000562118.1:n.599T>C | ||
| ENST00000562836.5:n.2452T>C | ||
| ENST00000566510.5:c.*1047T>C | ENSP00000458139.1:n.*1047T>C | |
| ENST00000566612.5:c.*621T>C | ENSP00000454782.1:n.*621T>C | |
| ENST00000611625.4:c.2444T>C | ENSP00000481063.1:p.Val815Ala | |
| ENST00000612417.4:c.1853+3185T>C | ENSP00000478360.1:n.1853+3185T>C | |
| ENST00000621016.4:c.1866-4464T>C | ENSP00000480664.1:n.1866-4464T>C | |
| NM_004360.3:c.2381T>C , LRG_301t1:c.2381T>C | NP_004351.1:p.Val794Ala | |
| XM_011523488.1:c.1646T>C | XP_011521790.1:p.Val549Ala | |
| XM_011523489.1:c.1646T>C | XP_011521791.1:p.Val549Ala | |
| NM_001317184.1:c.2198T>C | NP_001304113.1:p.Val733Ala | |
| NM_001317185.1:c.833T>C | NP_001304114.1:p.Val278Ala | |
| NM_001317186.1:c.416T>C | NP_001304115.1:p.Val139Ala | |
| NM_004360.4:c.2381T>C | NP_004351.1:p.Val794Ala | |
| NM_004360.5:c.2381T>C MANE Select | NP_004351.1:p.Val794Ala | |
| NM_001317184.2:c.2198T>C | NP_001304113.1:p.Val733Ala | |
| NM_001317185.2:c.833T>C | NP_001304114.1:p.Val278Ala | |
| NM_001317186.2:c.416T>C | NP_001304115.1:p.Val139Ala |