Linked Data
ClinVar Variation Id:
1164862
ClinVar RCV Id:
RCV001511383
dbSNP Id:
rs11542009
ExAC:
3:9517369 C / T
gnomAD v2:
3-9517369-C-T
gnomAD v3:
3-9475685-C-T
gnomAD v4:
3-9475685-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.9475685C>T , CM000665.2:g.9475685C>T | GRCh38 |
| NC_000003.11:g.9517369C>T , CM000665.1:g.9517369C>T | GRCh37 |
| NC_000003.10:g.9492369C>T | NCBI36 |
| NG_034132.1:g.82986C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682236.1:n.2878C>T | ||
| ENST00000682536.1:c.4019C>T | ENSP00000507956.1:p.Thr1340Ile | |
| ENST00000687014.1:n.4912C>T | ||
| ENST00000689167.1:n.2303C>T | ||
| ENST00000693430.1:n.6165C>T | ||
| ENST00000402198.7:c.3923C>T MANE Select | ENSP00000385852.2:p.Thr1308Ile | |
| ENST00000663774.1:c.*4069C>T | ENSP00000499452.1:n.*4069C>T | |
| ENST00000665872.1:c.*3992C>T | ENSP00000499600.1:n.*3992C>T | |
| ENST00000666307.1:c.*4297C>T | ENSP00000499402.1:n.*4297C>T | |
| ENST00000670063.1:c.*4028C>T | ENSP00000499725.1:n.*4028C>T | |
| ENST00000302463.10:c.3629C>T | ENSP00000302028.6:p.Thr1210Ile | |
| ENST00000399686.6:c.2722+529C>T | ||
| ENST00000402198.5:c.3923C>T | ENSP00000385852.1:p.Thr1308Ile | |
| ENST00000406341.5:c.3923C>T | ENSP00000383939.1:p.Thr1308Ile | |
| ENST00000407969.5:c.3980C>T | ENSP00000384114.1:p.Thr1327Ile | |
| ENST00000413704.5:c.2959C>T | ||
| ENST00000459941.1:n.1054C>T | ||
| ENST00000466242.5:n.3264C>T | ||
| ENST00000493918.5:n.4087C>T | ||
| NM_001080517.2:c.3923C>T | NP_001073986.1:p.Thr1308Ile | |
| NM_001292043.1:c.3629C>T | NP_001278972.1:p.Thr1210Ile | |
| XM_005265301.1:c.3980C>T | XP_005265358.1:p.Thr1327Ile | |
| XM_005265303.1:c.3923C>T | XP_005265360.1:p.Thr1308Ile | |
| XM_011533920.1:c.4097C>T | XP_011532222.1:p.Thr1366Ile | |
| XM_011533921.1:c.4097C>T | XP_011532223.1:p.Thr1366Ile | |
| XM_011533922.1:c.4076C>T | XP_011532224.1:p.Thr1359Ile | |
| XM_011533923.1:c.4076C>T | XP_011532225.1:p.Thr1359Ile | |
| XM_011533924.1:c.4076C>T | XP_011532226.1:p.Thr1359Ile | |
| XM_011533925.1:c.4058C>T | XP_011532227.1:p.Thr1353Ile | |
| XM_011533926.1:c.4040C>T | XP_011532228.1:p.Thr1347Ile | |
| XM_011533927.1:c.4040C>T | XP_011532229.1:p.Thr1347Ile | |
| XM_011533928.1:c.4019C>T | XP_011532230.1:p.Thr1340Ile | |
| XM_011533929.1:c.4001C>T | XP_011532231.1:p.Thr1334Ile | |
| XM_011533930.1:c.3962C>T | XP_011532232.1:p.Thr1321Ile | |
| XM_011533931.1:c.3686C>T | XP_011532233.1:p.Thr1229Ile | |
| XM_011533932.1:c.3647C>T | XP_011532234.1:p.Thr1216Ile | |
| XM_011533933.1:c.3647C>T | XP_011532235.1:p.Thr1216Ile | |
| NM_001349451.1:c.3629C>T | NP_001336380.1:p.Thr1210Ile | |
| XM_011533921.2:c.4097C>T | XP_011532223.1:p.Thr1366Ile | |
| XM_017006767.1:c.4097C>T | XP_016862256.1:p.Thr1366Ile | |
| XM_017006768.2:c.4076C>T | XP_016862257.1:p.Thr1359Ile | |
| XM_017006770.1:c.4040C>T | XP_016862259.1:p.Thr1347Ile | |
| XM_017006771.1:c.4037C>T | XP_016862260.1:p.Thr1346Ile | |
| XM_017006772.1:c.4001C>T | XP_016862261.1:p.Thr1334Ile | |
| XM_017006773.1:c.4001C>T | XP_016862262.1:p.Thr1334Ile | |
| XM_017006774.1:c.3980C>T | XP_016862263.1:p.Thr1327Ile | |
| XM_017006775.1:c.3944C>T | XP_016862264.1:p.Thr1315Ile | |
| XM_017006776.1:c.3686C>T | XP_016862265.1:p.Thr1229Ile | |
| XM_017006777.1:c.3686C>T | XP_016862266.1:p.Thr1229Ile | |
| XM_017006778.1:c.3686C>T | XP_016862267.1:p.Thr1229Ile | |
| XM_017006779.1:c.3647C>T | XP_016862268.1:p.Thr1216Ile | |
| XM_017006780.1:c.3647C>T | XP_016862269.1:p.Thr1216Ile | |
| XM_017006783.1:c.3419C>T | XP_016862272.1:p.Thr1140Ile | |
| XM_024453620.1:c.4058C>T | XP_024309388.1:p.Thr1353Ile | |
| XM_024453621.1:c.3734C>T | XP_024309389.1:p.Thr1245Ile | |
| XR_001740195.2:n.8306C>T | ||
| NM_001080517.3:c.3923C>T MANE Select | NP_001073986.1:p.Thr1308Ile | |
| NM_001292043.2:c.3629C>T | NP_001278972.1:p.Thr1210Ile | |
| NM_001349451.2:c.3629C>T | NP_001336380.1:p.Thr1210Ile |