Linked Data
ClinVar Variation Id:
297789
dbSNP Id:
rs375485412
ExAC:
1:5925255 G / A
gnomAD v2:
1-5925255-G-A
gnomAD v3:
1-5865195-G-A
gnomAD v4:
1-5865195-G-A
COSMIC:
COSM911147
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.5865195G>A , CM000663.2:g.5865195G>A | GRCh38 |
| NC_000001.10:g.5925255G>A , CM000663.1:g.5925255G>A | GRCh37 |
| NC_000001.9:g.5847842G>A | NCBI36 |
| NG_011724.2:g.132277C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378156.9:c.3723C>T MANE Select | ENSP00000367398.4:p.Val1241= | |
| ENST00000378156.8:c.3723C>T | ENSP00000367398.4:p.Val1241= | |
| ENST00000378161.5:n.1986C>T | ||
| ENST00000378169.7:c.*2624C>T | ENSP00000367411.3:n.*2624C>T | |
| ENST00000460696.1:n.1887C>T | ||
| ENST00000478423.6:n.3455C>T | ||
| ENST00000489180.6:c.*1534C>T | ENSP00000423747.1:n.*1534C>T | |
| NM_001291593.1:c.2184C>T | NP_001278522.1:p.Val728= | |
| NM_001291594.1:c.2187C>T | NP_001278523.1:p.Val729= | |
| NM_015102.4:c.3723C>T | NP_055917.1:p.Val1241= | |
| NR_111987.1:n.4538C>T | ||
| XM_006710563.2:c.3723C>T | XP_006710626.1:p.Val1241= | |
| XM_006710565.2:c.3723C>T | XP_006710628.1:p.Val1241= | |
| XM_011541213.1:c.3720C>T | XP_011539515.1:p.Val1240= | |
| XM_011541214.1:c.3681C>T | XP_011539516.1:p.Val1227= | |
| XM_011541215.1:c.3612C>T | XP_011539517.1:p.Val1204= | |
| XM_011541216.1:c.3723C>T | XP_011539518.1:p.Val1241= | |
| XM_011541217.1:c.3723C>T | XP_011539519.1:p.Val1241= | |
| XM_011541218.1:c.3723C>T | XP_011539520.1:p.Val1241= | |
| XM_011541219.1:c.3669C>T | XP_011539521.1:p.Val1223= | |
| XM_011541220.1:c.3645-678C>T | XP_011539522.1:n.3645-678C>T | |
| XM_006710563.3:c.3723C>T | XP_006710626.1:p.Val1241= | |
| XM_011541216.2:c.3723C>T | XP_011539518.1:p.Val1241= | |
| XM_011541217.2:c.3723C>T | XP_011539519.1:p.Val1241= | |
| XM_011541218.2:c.3723C>T | XP_011539520.1:p.Val1241= | |
| XM_017000996.1:c.3678C>T | XP_016856485.1:p.Val1226= | |
| XM_017000997.1:c.3723C>T | XP_016856486.1:p.Val1241= | |
| XM_017000998.1:c.3645-85C>T | XP_016856487.1:n.3645-85C>T | |
| XM_017000999.1:c.3195C>T | XP_016856488.1:p.Val1065= | |
| XM_017001000.2:c.3195C>T | XP_016856489.1:p.Val1065= | |
| XM_017001001.1:c.2925C>T | XP_016856490.1:p.Val975= | |
| XM_017001003.1:c.2184C>T | XP_016856492.1:p.Val728= | |
| XR_001737114.1:n.3683-678C>T | ||
| XR_001737115.1:n.3574C>T | ||
| NM_015102.5:c.3723C>T MANE Select | NP_055917.1:p.Val1241= | |
| NM_001291593.2:c.2184C>T | NP_001278522.1:p.Val728= | |
| NM_001291594.2:c.2187C>T | NP_001278523.1:p.Val729= | |
| NR_111987.2:n.4490C>T |