Linked Data
ClinVar Variation Id:
377826
dbSNP Id:
rs774640110
ExAC:
6:52344529 C / T
gnomAD v2:
6-52344529-C-T
gnomAD v3:
6-52479731-C-T
gnomAD v4:
6-52479731-C-T
COSMIC:
COSM3777751
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.52479731C>T , CM000668.2:g.52479731C>T | GRCh38 |
| NC_000006.11:g.52344529C>T , CM000668.1:g.52344529C>T | GRCh37 |
| NC_000006.10:g.52452488C>T | NCBI36 |
| NG_016760.1:g.64536C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371068.11:c.1584C>T MANE Select | ENSP00000360107.4:p.Leu528= | |
| ENST00000480623.6:c.1584C>T | ENSP00000434498.2:p.Leu528= | |
| ENST00000635760.1:c.1260C>T | ENSP00000489765.1:p.Leu420= | |
| ENST00000635812.1:c.*885C>T | ENSP00000490859.1:n.*885C>T | |
| ENST00000635866.1:c.*1453C>T | ENSP00000489866.1:n.*1453C>T | |
| ENST00000635911.1:n.3102C>T | ||
| ENST00000635984.1:c.1260C>T | ENSP00000489921.1:p.Leu420= | |
| ENST00000635996.1:c.1584C>T | ENSP00000490256.1:p.Leu528= | |
| ENST00000636107.1:c.1584C>T | ENSP00000489680.1:p.Leu528= | |
| ENST00000636311.1:n.1478C>T | ||
| ENST00000636343.1:c.1250C>T | ||
| ENST00000636379.1:c.1296C>T | ENSP00000490622.1:p.Leu432= | |
| ENST00000636398.1:c.1284C>T | ENSP00000489654.1:n.1284C>T | |
| ENST00000636489.1:c.1527C>T | ENSP00000489998.1:p.Leu509= | |
| ENST00000636616.1:n.1145C>T | ||
| ENST00000636702.1:c.1554C>T | ENSP00000489623.1:p.Leu518= | |
| ENST00000636954.1:c.1527C>T | ENSP00000489966.1:p.Leu509= | |
| ENST00000637089.1:c.1584C>T | ENSP00000489854.1:p.Leu528= | |
| ENST00000637121.1:n.1386C>T | ||
| ENST00000637263.1:c.1584C>T | ENSP00000489700.1:p.Leu528= | |
| ENST00000637340.1:n.3509C>T | ||
| ENST00000637353.1:c.1584C>T | ENSP00000490441.1:p.Leu528= | |
| ENST00000637602.1:c.*1285C>T | ENSP00000490074.1:n.*1285C>T | |
| ENST00000637849.1:n.1648C>T | ||
| ENST00000637892.1:n.1788C>T | ||
| ENST00000371068.9:c.1584C>T | ENSP00000360107.4:p.Leu528= | |
| ENST00000480623.5:c.*2004C>T | ENSP00000434498.1:n.*2004C>T | |
| ENST00000538167.2:c.1527C>T | ENSP00000444521.1:p.Leu509= | |
| NM_001172420.1:c.1527C>T | NP_001165891.1:p.Leu509= | |
| NM_018100.3:c.1584C>T | NP_060570.2:p.Leu528= | |
| NR_033327.1:n.3056C>T | ||
| NM_018100.4:c.1584C>T MANE Select | NP_060570.2:p.Leu528= | |
| NM_001172420.2:c.1527C>T | NP_001165891.1:p.Leu509= | |
| NR_033327.2:n.2910C>T |