Linked Data
dbSNP Id:
rs764886832
ExAC:
3:123426835 G / A
gnomAD v2:
3-123426835-G-A
gnomAD v3:
3-123707988-G-A
gnomAD v4:
3-123707988-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.123707988G>A , CM000665.2:g.123707988G>A | GRCh38 |
| NC_000003.11:g.123426835G>A , CM000665.1:g.123426835G>A | GRCh37 |
| NC_000003.10:g.124909525G>A | NCBI36 |
| NG_029111.1:g.181315C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000346322.10:c.1949C>T | ENSP00000320622.6:p.Thr650Ile | |
| ENST00000686406.1:c.2156C>T | ENSP00000509044.1:p.Thr719Ile | |
| ENST00000686761.1:c.2156C>T | ENSP00000508758.1:p.Thr719Ile | |
| ENST00000686822.1:n.2050C>T | ||
| ENST00000687848.1:c.2186C>T | ENSP00000508761.1:p.Thr729Ile | |
| ENST00000690457.1:c.1394C>T | ENSP00000508777.1:p.Thr465Ile | |
| ENST00000693689.1:c.1949C>T | ENSP00000510503.1:p.Thr650Ile | |
| ENST00000360304.8:c.2156C>T MANE Select | ENSP00000353452.3:p.Thr719Ile | |
| ENST00000346322.9:c.1949C>T | ENSP00000320622.5:p.Thr650Ile | |
| ENST00000354792.9:c.1949C>T | ENSP00000346846.6:p.Thr650Ile | |
| ENST00000359169.5:c.2156C>T | ENSP00000352088.1:p.Thr719Ile | |
| ENST00000360304.7:c.2156C>T | ENSP00000353452.3:p.Thr719Ile | |
| ENST00000360772.7:c.2156C>T | ENSP00000354004.3:p.Thr719Ile | |
| ENST00000464489.5:c.*1735C>T | ENSP00000417798.1:n.*1735C>T | |
| ENST00000475616.5:c.2156C>T | ENSP00000418335.1:p.Thr719Ile | |
| NM_053025.3:c.2156C>T | NP_444253.3:p.Thr719Ile | |
| NM_053026.3:c.1949C>T | NP_444254.3:p.Thr650Ile | |
| NM_053027.3:c.2156C>T | NP_444255.3:p.Thr719Ile | |
| NM_053028.3:c.1949C>T | NP_444256.3:p.Thr650Ile | |
| XM_011512860.1:c.2156C>T | XP_011511162.1:p.Thr719Ile | |
| XM_011512861.1:c.2156C>T | XP_011511163.1:p.Thr719Ile | |
| XM_011512862.1:c.1628C>T | XP_011511164.1:p.Thr543Ile | |
| XR_241556.2:n.313+3979G>A | ||
| XR_427403.2:n.406+3979G>A | ||
| XR_924414.1:n.406+3979G>A | ||
| XR_924415.1:n.403+3979G>A | ||
| XR_924416.1:n.230+3979G>A | ||
| XR_924417.1:n.226+3979G>A | ||
| XR_924418.1:n.406+3979G>A | ||
| NM_001321309.1:c.1628C>T | NP_001308238.1:p.Thr543Ile | |
| XM_011512860.3:c.2186C>T | XP_011511162.2:p.Thr729Ile | |
| XM_011512861.3:c.2186C>T | XP_011511163.2:p.Thr729Ile | |
| XM_024453532.1:c.2186C>T | XP_024309300.1:p.Thr729Ile | |
| XM_024453533.1:c.2156C>T | XP_024309301.1:p.Thr719Ile | |
| XM_024453534.1:c.1979C>T | XP_024309302.1:p.Thr660Ile | |
| XM_024453535.1:c.1949C>T | XP_024309303.1:p.Thr650Ile | |
| XM_024453536.1:c.2156C>T | XP_024309304.1:p.Thr719Ile | |
| XM_024453537.1:c.2156C>T | XP_024309305.1:p.Thr719Ile | |
| XR_001740871.2:n.406+3979G>A | ||
| XR_427403.4:n.406+3979G>A | ||
| XR_924414.3:n.406+3979G>A | ||
| XR_924417.3:n.251+3979G>A | ||
| XR_924418.3:n.406+3979G>A | ||
| NM_001321309.2:c.1628C>T | NP_001308238.1:p.Thr543Ile | |
| NM_053025.4:c.2156C>T MANE Select | NP_444253.3:p.Thr719Ile | |
| NM_053026.4:c.1949C>T | NP_444254.3:p.Thr650Ile | |
| NM_053027.4:c.2156C>T | NP_444255.3:p.Thr719Ile | |
| NM_053028.4:c.1949C>T | NP_444256.3:p.Thr650Ile |