Linked Data
ClinVar Variation Id:
2139457
ClinVar RCV Id:
RCV003066604
dbSNP Id:
rs1293948745
gnomAD v2:
9-35801121-T-C
gnomAD v3:
9-35801124-T-C
gnomAD v4:
9-35801124-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.35801124T>C , CM000671.2:g.35801124T>C | GRCh38 |
| NC_000009.11:g.35801121T>C , CM000671.1:g.35801121T>C | GRCh37 |
| NC_000009.10:g.35791121T>C | NCBI36 |
| NG_009249.1:g.13716T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000448821.6:c.1406T>C | ENSP00000402902.2:p.Met469Thr | |
| ENST00000685871.1:c.1406T>C | ENSP00000509964.1:p.Met469Thr | |
| ENST00000686159.1:n.1445T>C | ||
| ENST00000686486.1:n.414T>C | ||
| ENST00000687302.1:n.1492T>C | ||
| ENST00000687357.1:c.1406T>C | ENSP00000509549.1:p.Met469Thr | |
| ENST00000687625.1:n.561T>C | ||
| ENST00000687787.1:c.1406T>C | ENSP00000509440.1:p.Met469Thr | |
| ENST00000688201.1:n.1438T>C | ||
| ENST00000688226.1:n.1338T>C | ||
| ENST00000688869.1:n.1712T>C | ||
| ENST00000689788.1:c.1200T>C | ENSP00000508973.1:n.1200T>C | |
| ENST00000689898.1:c.1410T>C | ENSP00000509651.1:p.His470= | |
| ENST00000690070.1:c.1406T>C | ENSP00000509654.1:p.Met469Thr | |
| ENST00000690267.1:c.1270T>C | ENSP00000510432.1:n.1270T>C | |
| ENST00000690552.1:n.1267T>C | ||
| ENST00000691138.1:n.1267T>C | ||
| ENST00000691969.1:c.981T>C | ENSP00000510244.1:n.981T>C | |
| ENST00000692232.1:n.2562T>C | ||
| ENST00000692233.1:c.1270T>C | ENSP00000509698.1:n.1270T>C | |
| ENST00000692380.1:n.561T>C | ||
| ENST00000692447.1:n.2522T>C | ||
| ENST00000693094.1:c.1406T>C | ENSP00000510161.1:p.Met469Thr | |
| ENST00000342694.7:c.1406T>C MANE Select | ENSP00000341083.2:p.Met469Thr | |
| ENST00000342694.6:c.1406T>C | ENSP00000341083.2:p.Met469Thr | |
| ENST00000464810.5:n.1406T>C | ||
| NM_003995.3:c.1406T>C | NP_003986.2:p.Met469Thr | |
| XM_005251478.3:c.1406T>C | XP_005251535.1:p.Met469Thr | |
| XM_005251479.3:c.419T>C | XP_005251536.1:p.Met140Thr | |
| XM_006716778.2:c.1406T>C | XP_006716841.1:p.Met469Thr | |
| XM_011517889.1:c.419T>C | XP_011516191.1:p.Met140Thr | |
| XM_011517890.1:c.419T>C | XP_011516192.1:p.Met140Thr | |
| XM_011517891.1:c.419T>C | XP_011516193.1:p.Met140Thr | |
| XM_011517892.1:c.419T>C | XP_011516194.1:p.Met140Thr | |
| XM_011517893.1:c.419T>C | XP_011516195.1:p.Met140Thr | |
| XM_011517894.1:c.419T>C | XP_011516196.1:p.Met140Thr | |
| XM_011517895.1:c.2T>C | XP_011516197.1:p.Met1Thr | |
| XM_024447556.1:c.1406T>C | XP_024303324.1:p.Met469Thr | |
| XM_024447557.1:c.1406T>C | XP_024303325.1:p.Met469Thr | |
| XM_024447558.1:c.419T>C | XP_024303326.1:p.Met140Thr | |
| XM_024447559.1:c.2T>C | XP_024303327.1:p.Met1Thr | |
| XM_024447560.1:c.2T>C | XP_024303328.1:p.Met1Thr | |
| XM_024447561.1:c.2T>C | XP_024303329.1:p.Met1Thr | |
| NM_003995.4:c.1406T>C MANE Select | NP_003986.2:p.Met469Thr | |
| NM_001378923.1:c.1406T>C | NP_001365852.1:p.Met469Thr |