Linked Data
ClinVar Variation Id:
348565
ClinVar RCV Id:
RCV000283666
dbSNP Id:
rs774809755
ExAC:
4:2822441 C / T
gnomAD v2:
4-2822441-C-T
gnomAD v3:
4-2820714-C-T
gnomAD v4:
4-2820714-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.2820714C>T , CM000666.2:g.2820714C>T | GRCh38 |
| NC_000004.11:g.2822441C>T , CM000666.1:g.2822441C>T | GRCh37 |
| NC_000004.10:g.2792239C>T | NCBI36 |
| NG_011609.1:g.32692C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000435136.8:c.181C>T | ENSP00000403231.3:p.Leu61= | |
| ENST00000503393.8:c.97C>T MANE Select | ENSP00000422168.3:p.Leu33= | |
| ENST00000511747.6:c.268C>T | ENSP00000424846.2:p.Leu90= | |
| ENST00000356331.9:c.97C>T | ENSP00000348685.5:p.Leu33= | |
| ENST00000435136.6:c.97C>T | ENSP00000403231.2:p.Leu33= | |
| ENST00000442312.6:c.181C>T | ENSP00000388152.2:p.Leu61= | |
| ENST00000452765.6:c.97C>T | ENSP00000409746.2:p.Leu33= | |
| ENST00000502260.5:c.97C>T | ENSP00000425537.1:p.Leu33= | |
| ENST00000503219.5:c.97C>T | ENSP00000422796.1:p.Leu33= | |
| ENST00000503393.6:c.268C>T | ENSP00000422168.2:p.Leu90= | |
| ENST00000504294.5:c.97C>T | ENSP00000423275.1:p.Leu33= | |
| ENST00000506932.1:n.46C>T | ||
| ENST00000508385.5:c.97C>T | ENSP00000424917.1:p.Leu33= | |
| ENST00000509677.5:n.456C>T | ||
| ENST00000510074.5:n.205C>T | ||
| ENST00000511185.5:n.278C>T | ||
| ENST00000511237.5:n.205C>T | ||
| ENST00000511663.5:n.152C>T | ||
| ENST00000511747.5:c.97C>T | ENSP00000424846.1:p.Leu33= | |
| ENST00000512014.5:c.97C>T | ENSP00000424105.1:p.Leu33= | |
| ENST00000512131.5:n.168C>T | ||
| ENST00000513020.5:c.97C>T | ENSP00000424072.1:p.Leu33= | |
| ENST00000513095.5:c.97C>T | ENSP00000423823.1:p.Leu33= | |
| ENST00000515737.5:c.97C>T | ENSP00000422605.1:p.Leu33= | |
| NM_001122681.1:c.97C>T | NP_001116153.1:p.Leu33= | |
| NM_001145855.1:c.181C>T | NP_001139327.1:p.Leu61= | |
| NM_001145856.1:c.268C>T | NP_001139328.1:p.Leu90= | |
| NM_003023.4:c.97C>T | NP_003014.3:p.Leu33= | |
| XM_005247998.3:c.106C>T | XP_005248055.1:p.Leu36= | |
| XM_005247999.3:c.97C>T | XP_005248056.1:p.Leu33= | |
| XM_011513547.1:c.268C>T | XP_011511849.1:p.Leu90= | |
| XM_011513548.1:c.97C>T | XP_011511850.1:p.Leu33= | |
| XM_011513549.1:c.97C>T | XP_011511851.1:p.Leu33= | |
| XM_011513550.1:c.97C>T | XP_011511852.1:p.Leu33= | |
| XM_011513551.1:c.97C>T | XP_011511853.1:p.Leu33= | |
| XM_011513552.1:c.-250C>T | XP_011511854.1:n.-250C>T | |
| XM_011513553.1:c.-662C>T | XP_011511855.1:n.-662C>T | |
| XM_011513554.1:c.97C>T | XP_011511856.1:p.Leu33= | |
| XM_011513555.1:c.97C>T | XP_011511857.1:p.Leu33= | |
| XM_011513556.1:c.97C>T | XP_011511858.1:p.Leu33= | |
| XR_924990.1:n.101C>T | ||
| NM_001122681.2:c.97C>T MANE Select | NP_001116153.1:p.Leu33= | |
| NM_001145855.2:c.181C>T | NP_001139327.1:p.Leu61= | |
| NM_001145856.2:c.268C>T | NP_001139328.1:p.Leu90= |