Linked Data
ClinVar Variation Id:
1910256
ClinVar RCV Id:
RCV002593134
dbSNP Id:
rs986284106
gnomAD v3:
8-60860911-C-T
gnomAD v4:
8-60860911-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.60860911C>T , CM000670.2:g.60860911C>T | GRCh38 |
| NC_000008.10:g.61773470C>T , CM000670.1:g.61773470C>T | GRCh37 |
| NC_000008.9:g.61936024C>T | NCBI36 |
| NG_007009.1:g.187132C>T , LRG_176:g.187132C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695850.1:n.792C>T | ||
| ENST00000695853.1:c.*675C>T | ENSP00000512218.1:n.*675C>T | |
| ENST00000423902.7:c.7616C>T MANE Select | ENSP00000392028.1:p.Ala2539Val | |
| ENST00000423902.6:c.7616C>T | ENSP00000392028.1:p.Ala2539Val | |
| ENST00000524602.5:c.1717-1318C>T | ENSP00000437061.1:n.1717-1318C>T | |
| ENST00000531695.1:n.40C>T | ||
| ENST00000618450.1:n.8C>T | ||
| NM_001316690.1:c.1717-1318C>T | NP_001303619.1:n.1717-1318C>T | |
| NM_017780.3:c.7616C>T | NP_060250.2:p.Ala2539Val | |
| XM_011517553.1:c.7706C>T | XP_011515855.1:p.Ala2569Val | |
| XM_011517554.1:c.7706C>T | XP_011515856.1:p.Ala2569Val | |
| XM_011517555.1:c.7703C>T | XP_011515857.1:p.Ala2568Val | |
| XM_011517556.1:c.7699-1285C>T | XP_011515858.1:n.7699-1285C>T | |
| XM_011517557.1:c.5693C>T | XP_011515859.1:p.Ala1898Val | |
| XM_011517558.1:c.5243C>T | XP_011515860.1:p.Ala1748Val | |
| XM_011517559.1:c.4451C>T | XP_011515861.1:p.Ala1484Val | |
| XM_011517553.2:c.7706C>T | XP_011515855.1:p.Ala2569Val | |
| XM_011517554.3:c.7706C>T | XP_011515856.1:p.Ala2569Val | |
| XM_011517555.2:c.7703C>T | XP_011515857.1:p.Ala2568Val | |
| XM_017013612.1:c.7706C>T | XP_016869101.1:p.Ala2569Val | |
| XM_017013613.1:c.7613C>T | XP_016869102.1:p.Ala2538Val | |
| NM_017780.4:c.7616C>T MANE Select | NP_060250.2:p.Ala2539Val |