Linked Data
ClinVar Variation Id:
1109321
ClinVar RCV Id:
RCV001435153
dbSNP Id:
rs756161296
ExAC:
X:107865036 C / T
gnomAD v2:
X-107865036-C-T
gnomAD v3:
X-108621806-C-T
gnomAD v4:
X-108621806-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.108621806C>T , CM000685.2:g.108621806C>T | GRCh38 |
| NC_000023.10:g.107865036C>T , CM000685.1:g.107865036C>T | GRCh37 |
| NC_000023.9:g.107751692C>T | NCBI36 |
| NG_011977.1:g.186883C>T | |
| NG_011977.2:g.186883C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000328300.11:c.2681C>T MANE Select | ENSP00000331902.7:p.Thr894Ile | |
| ENST00000361603.7:c.2681C>T | ENSP00000354505.2:p.Thr894Ile | |
| ENST00000328300.10:c.2681C>T | ENSP00000331902.6:p.Thr894Ile | |
| ENST00000361603.6:c.2681C>T | ENSP00000354505.2:p.Thr894Ile | |
| ENST00000483338.1:n.2137C>T | ||
| NM_000495.4:c.2681C>T | NP_000486.1:p.Thr894Ile | |
| NM_033380.2:c.2681C>T | NP_203699.1:p.Thr894Ile | |
| XM_005262070.2:c.2681C>T | XP_005262127.1:p.Thr894Ile | |
| XM_005262072.3:c.2681C>T | XP_005262129.1:p.Thr894Ile | |
| XM_006724616.2:c.2681C>T | XP_006724679.1:p.Thr894Ile | |
| XM_011530849.1:c.2357C>T | XP_011529151.1:p.Thr786Ile | |
| XM_011530850.1:c.2681C>T | XP_011529152.1:p.Thr894Ile | |
| XM_011530851.1:c.254C>T | XP_011529153.1:p.Thr85Ile | |
| XM_011530849.2:c.2696C>T | XP_011529151.2:p.Thr899Ile | |
| XM_017029259.2:c.2696C>T | XP_016884748.1:p.Thr899Ile | |
| XM_017029260.1:c.2696C>T | XP_016884749.1:p.Thr899Ile | |
| XM_017029261.1:c.2696C>T | XP_016884750.1:p.Thr899Ile | |
| XM_017029262.2:c.2696C>T | XP_016884751.1:p.Thr899Ile | |
| XM_017029263.2:c.1016C>T | XP_016884752.1:p.Thr339Ile | |
| NM_000495.5:c.2681C>T | NP_000486.1:p.Thr894Ile | |
| NM_033380.3:c.2681C>T MANE Select | NP_203699.1:p.Thr894Ile |