Linked Data
ClinVar Variation Id:
2933952
ClinVar RCV Id:
RCV003793510
dbSNP Id:
rs753659359
ExAC:
11:22281110 C / T
gnomAD v2:
11-22281110-C-T
gnomAD v4:
11-22259564-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.22259564C>T , CM000673.2:g.22259564C>T | GRCh38 |
| NC_000011.9:g.22281110C>T , CM000673.1:g.22281110C>T | GRCh37 |
| NC_000011.8:g.22237686C>T | NCBI36 |
| NG_015844.1:g.71389C>T , LRG_868:g.71389C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000682266.1:c.1003C>T | ENSP00000507766.1:p.Leu335= | |
| ENST00000682341.1:c.1411C>T | ENSP00000508251.1:p.Leu471= | |
| ENST00000683197.1:c.1411C>T | ENSP00000507641.1:p.Leu471= | |
| ENST00000683411.1:c.1003C>T | ENSP00000508397.1:p.Leu335= | |
| ENST00000683437.1:c.1003C>T | ENSP00000508408.1:p.Leu335= | |
| ENST00000683613.1:n.2447C>T | ||
| ENST00000684663.1:c.1408C>T | ENSP00000508009.1:p.Leu470= | |
| ENST00000324559.9:c.1453C>T MANE Select | ENSP00000315371.9:p.Leu485= | |
| ENST00000648804.1:n.1788C>T | ||
| ENST00000324559.8:c.1453C>T | ENSP00000315371.8:p.Leu485= | |
| NM_001142649.1:c.1450C>T | NP_001136121.1:p.Leu484= | |
| NM_213599.2:c.1453C>T , LRG_868t1:c.1453C>T | NP_998764.1:p.Leu485= | |
| XM_005252820.2:c.1411C>T | XP_005252877.2:p.Leu471= | |
| XM_005252821.2:c.1408C>T | XP_005252878.2:p.Leu470= | |
| XM_005252822.3:c.1375C>T | XP_005252879.1:p.Leu459= | |
| XM_005252823.3:c.1372C>T | XP_005252880.1:p.Leu458= | |
| XM_011519949.1:c.1360C>T | XP_011518251.1:p.Leu454= | |
| XM_005252820.3:c.1411C>T | XP_005252877.2:p.Leu471= | |
| XM_005252821.3:c.1408C>T | XP_005252878.2:p.Leu470= | |
| XM_005252822.4:c.1375C>T | XP_005252879.1:p.Leu459= | |
| XM_011519949.2:c.1360C>T | XP_011518251.1:p.Leu454= | |
| NM_001142649.2:c.1450C>T | NP_001136121.1:p.Leu484= | |
| NM_213599.3:c.1453C>T MANE Select | NP_998764.1:p.Leu485= |