Linked Data
ClinVar Variation Id:
837948
ClinVar RCV Id:
RCV001039391
dbSNP Id:
rs1432542467
gnomAD v4:
6-7580086-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.7580086T>C , CM000668.2:g.7580086T>C | GRCh38 |
| NC_000006.11:g.7580319T>C , CM000668.1:g.7580319T>C | GRCh37 |
| NC_000006.10:g.7525318T>C | NCBI36 |
| NG_008803.1:g.43450T>C , LRG_423:g.43450T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000710359.1:c.3896T>C | ENSP00000518230.1:p.Met1299Thr | |
| ENST00000379802.8:c.3896T>C MANE Select | ENSP00000369129.3:p.Met1299Thr | |
| ENST00000379802.7:c.3896T>C | ENSP00000369129.3:p.Met1299Thr | |
| ENST00000418664.2:c.3582+314T>C | ENSP00000396591.2:n.3582+314T>C | |
| NM_001008844.1:c.3582+314T>C | NP_001008844.1:n.3582+314T>C | |
| NM_004415.2:c.3896T>C , LRG_423t1:c.3896T>C | NP_004406.2:p.Met1299Thr | |
| XM_011514323.1:c.3896T>C | XP_011512625.1:p.Met1299Thr | |
| NM_001008844.2:c.3582+314T>C | NP_001008844.1:n.3582+314T>C | |
| NM_001319034.1:c.3896T>C | NP_001305963.1:p.Met1299Thr | |
| NM_004415.3:c.3896T>C | NP_004406.2:p.Met1299Thr | |
| NM_004415.4:c.3896T>C MANE Select | NP_004406.2:p.Met1299Thr | |
| NM_001008844.3:c.3582+314T>C | NP_001008844.1:n.3582+314T>C | |
| NM_001319034.2:c.3896T>C | NP_001305963.1:p.Met1299Thr |