Linked Data
ClinVar Variation Id:
2077841
ClinVar RCV Id:
RCV002985730
dbSNP Id:
rs368357599
ExAC:
19:36595492 C / T
gnomAD v2:
19-36595492-C-T
gnomAD v3:
19-36104590-C-T
gnomAD v4:
19-36104590-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.36104590C>T , CM000681.2:g.36104590C>T | GRCh38 |
| NC_000019.9:g.36595492C>T , CM000681.1:g.36595492C>T | GRCh37 |
| NC_000019.8:g.41287332C>T | NCBI36 |
| NG_028101.1:g.54710C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000270301.12:c.4211C>T | ENSP00000270301.6:p.Pro1404Leu | |
| ENST00000401500.7:c.4226C>T MANE Select | ENSP00000384792.1:p.Pro1409Leu | |
| ENST00000587391.6:c.*4086C>T | ENSP00000465525.1:n.*4086C>T | |
| ENST00000679357.1:c.2306C>T | ||
| ENST00000679598.1:c.971C>T | ||
| ENST00000679682.1:c.4211C>T | ENSP00000506226.1:p.Pro1404Leu | |
| ENST00000679714.1:c.4220C>T | ENSP00000506627.1:p.Pro1407Leu | |
| ENST00000679757.1:c.3875C>T | ENSP00000505158.1:p.Pro1292Leu | |
| ENST00000679858.1:c.*3608C>T | ENSP00000505655.1:n.*3608C>T | |
| ENST00000680211.1:c.827C>T | ENSP00000506102.1:p.Pro276Leu | |
| ENST00000680280.1:n.1729C>T | ||
| ENST00000680349.1:n.2875C>T | ||
| ENST00000680403.1:c.4211C>T | ENSP00000505677.1:p.Pro1404Leu | |
| ENST00000680564.1:c.3977C>T | ENSP00000505582.1:p.Pro1326Leu | |
| ENST00000680590.1:c.*2606C>T | ENSP00000505350.1:n.*2606C>T | |
| ENST00000680597.1:c.959C>T | ||
| ENST00000680739.1:c.1241C>T | ||
| ENST00000680773.1:n.2727C>T | ||
| ENST00000680806.1:c.*3529C>T | ENSP00000506418.1:n.*3529C>T | |
| ENST00000680997.1:n.2158C>T | ||
| ENST00000681608.1:n.2071C>T | ||
| ENST00000681625.1:c.*1558C>T | ENSP00000505555.1:n.*1558C>T | |
| ENST00000681648.1:n.2277C>T | ||
| ENST00000270301.11:c.4211C>T | ENSP00000270301.6:p.Pro1404Leu | |
| ENST00000401500.6:c.4226C>T | ENSP00000384792.1:p.Pro1409Leu | |
| ENST00000587391.5:c.*4086C>T | ENSP00000465525.1:n.*4086C>T | |
| NM_001083961.1:c.4226C>T | NP_001077430.1:p.Pro1409Leu | |
| NM_173636.4:c.4211C>T | NP_775907.4:p.Pro1404Leu | |
| XM_005258809.2:c.4115C>T | XP_005258866.1:p.Pro1372Leu | |
| XM_011526837.1:c.4211C>T | XP_011525139.1:p.Pro1404Leu | |
| XM_011526838.1:c.3977C>T | XP_011525140.1:p.Pro1326Leu | |
| XM_011526839.1:c.3875C>T | XP_011525141.1:p.Pro1292Leu | |
| XM_011526840.1:c.3218C>T | XP_011525142.1:p.Pro1073Leu | |
| XM_011526841.1:c.2804C>T | XP_011525143.1:p.Pro935Leu | |
| XM_011526842.1:c.2657C>T | XP_011525144.1:p.Pro886Leu | |
| XM_011526843.1:c.1973C>T | XP_011525145.1:p.Pro658Leu | |
| XM_011526844.1:c.1973C>T | XP_011525146.1:p.Pro658Leu | |
| XM_011526840.2:c.3218C>T | XP_011525142.1:p.Pro1073Leu | |
| XM_011526841.2:c.2804C>T | XP_011525143.1:p.Pro935Leu | |
| XM_011526844.2:c.1973C>T | XP_011525146.1:p.Pro658Leu | |
| XM_017026665.1:c.4226C>T | XP_016882154.1:p.Pro1409Leu | |
| NM_001083961.2:c.4226C>T MANE Select | NP_001077430.1:p.Pro1409Leu | |
| NM_173636.5:c.4211C>T | NP_775907.4:p.Pro1404Leu |