Linked Data
ClinVar Variation Id:
508931
dbSNP Id:
rs145891535
ExAC:
11:66620777 G / A
gnomAD v2:
11-66620777-G-A
gnomAD v3:
11-66853306-G-A
gnomAD v4:
11-66853306-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.66853306G>A , CM000673.2:g.66853306G>A | GRCh38 |
| NC_000011.9:g.66620777G>A , CM000673.1:g.66620777G>A | GRCh37 |
| NC_000011.8:g.66377353G>A | NCBI36 |
| NG_008319.1:g.110071C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000393958.7:c.1446C>T | ENSP00000377530.2:p.Asp482= | |
| ENST00000393960.7:c.1446C>T MANE Select | ENSP00000377532.1:p.Asp482= | |
| ENST00000525476.2:n.290-3241C>T | ||
| ENST00000528224.2:c.1446C>T | ENSP00000498317.1:p.Asp482= | |
| ENST00000528403.6:c.1446C>T | ENSP00000498816.1:p.Asp482= | |
| ENST00000529047.6:c.1446C>T | ENSP00000435905.2:p.Asp482= | |
| ENST00000651036.1:c.1446C>T | ENSP00000498406.1:p.Asp482= | |
| ENST00000651469.1:c.1514C>T | ENSP00000498712.1:p.Thr505Met | |
| ENST00000651831.1:n.272C>T | ||
| ENST00000651854.1:c.1446C>T | ENSP00000498994.1:p.Asp482= | |
| ENST00000652125.1:c.1446C>T | ENSP00000498302.1:p.Asp482= | |
| ENST00000652387.1:n.309C>T | ||
| ENST00000393955.6:c.1446C>T | ENSP00000377527.2:p.Asp482= | |
| ENST00000393958.6:c.1446C>T | ENSP00000377530.2:p.Asp482= | |
| ENST00000393960.5:c.1446C>T | ENSP00000377532.1:p.Asp482= | |
| NM_000920.3:c.1446C>T | NP_000911.2:p.Asp482= | |
| NM_001040716.1:c.1446C>T | NP_001035806.1:p.Asp482= | |
| NM_022172.2:c.1446C>T | NP_071504.2:p.Asp482= | |
| XM_005274031.3:c.1446C>T | XP_005274088.1:p.Asp482= | |
| XM_005274032.3:c.1446C>T | XP_005274089.1:p.Asp482= | |
| XM_006718577.2:c.1446C>T | XP_006718640.1:p.Asp482= | |
| XM_006718578.2:c.1446C>T | XP_006718641.1:p.Asp482= | |
| XM_006718579.2:c.-76C>T | XP_006718642.1:n.-76C>T | |
| XM_011545085.1:c.1446C>T | XP_011543387.1:p.Asp482= | |
| XM_011545086.1:c.1446C>T | XP_011543388.1:p.Asp482= | |
| XM_011545087.1:c.150C>T | XP_011543389.1:p.Asp50= | |
| XM_011545088.1:c.81C>T | XP_011543390.1:p.Asp27= | |
| XM_005274031.4:c.1446C>T | XP_005274088.1:p.Asp482= | |
| XM_005274032.4:c.1446C>T | XP_005274089.1:p.Asp482= | |
| XM_006718578.3:c.1446C>T | XP_006718641.1:p.Asp482= | |
| XM_006718579.3:c.-76C>T | XP_006718642.1:n.-76C>T | |
| XM_011545086.2:c.1446C>T | XP_011543388.1:p.Asp482= | |
| XM_011545087.2:c.150C>T | XP_011543389.1:p.Asp50= | |
| XM_017017868.1:c.1446C>T | XP_016873357.1:p.Asp482= | |
| XM_017017869.1:c.1446C>T | XP_016873358.1:p.Asp482= | |
| XM_017017870.1:c.1446C>T | XP_016873359.1:p.Asp482= | |
| XM_017017871.1:c.1446C>T | XP_016873360.1:p.Asp482= | |
| XM_017017872.2:c.1446C>T | XP_016873361.1:p.Asp482= | |
| NM_000920.4:c.1446C>T | NP_000911.2:p.Asp482= | |
| NM_001040716.2:c.1446C>T MANE Select | NP_001035806.1:p.Asp482= | |
| NM_022172.3:c.1446C>T | NP_071504.2:p.Asp482= |