Linked Data
ClinVar Variation Id:
434735
ClinVar RCV Id:
RCV000501448
dbSNP Id:
rs777337799
gnomAD v2:
15-49030877-G-T
gnomAD v3:
15-48738680-G-T
gnomAD v4:
15-48738680-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48738680G>T , CM000677.2:g.48738680G>T | GRCh38 |
| NC_000015.9:g.49030877G>T , CM000677.1:g.49030877G>T | GRCh37 |
| NC_000015.8:g.46818169G>T | NCBI36 |
| NG_027518.1:g.77467C>A | |
| NG_027518.2:g.77467C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000380950.7:c.4702C>A MANE Select | ENSP00000370337.2:p.Leu1568Ile | |
| ENST00000380950.6:c.4702C>A | ENSP00000370337.2:p.Leu1568Ile | |
| ENST00000399334.7:c.4534C>A | ENSP00000382271.3:p.Leu1512Ile | |
| ENST00000561245.1:c.142+2951C>A | ENSP00000453591.1:n.142+2951C>A | |
| NM_001194998.1:c.4702C>A | NP_001181927.1:p.Leu1568Ile | |
| NM_014985.3:c.4534C>A | NP_055800.2:p.Leu1512Ile | |
| XM_006720437.2:c.4702C>A | XP_006720500.1:p.Leu1568Ile | |
| XM_011521373.1:c.4672C>A | XP_011519675.1:p.Leu1558Ile | |
| XM_011521374.1:c.4093+2921C>A | XP_011519676.1:n.4093+2921C>A | |
| XM_011521375.1:c.4064-1459C>A | XP_011519677.1:n.4064-1459C>A | |
| XM_011521376.1:c.4063+2951C>A | XP_011519678.1:n.4063+2951C>A | |
| XM_011521378.1:c.4063+2951C>A | XP_011519680.1:n.4063+2951C>A | |
| XM_011521380.1:c.2743C>A | XP_011519682.1:p.Leu915Ile | |
| XM_011521381.1:c.2737C>A | XP_011519683.1:p.Leu913Ile | |
| XR_931769.1:n.5029-1459C>A | ||
| XR_931770.1:n.5058+2921C>A | ||
| XR_931771.1:n.5058+2921C>A | ||
| XR_931772.1:n.5058+2921C>A | ||
| XR_931773.1:n.5058+2921C>A | ||
| XR_931774.1:n.5058+2921C>A | ||
| XR_931775.1:n.5028+2951C>A | ||
| XM_006720437.3:c.4702C>A | XP_006720500.1:p.Leu1568Ile | |
| XM_011521373.3:c.4672C>A | XP_011519675.1:p.Leu1558Ile | |
| XM_011521374.3:c.4093+2921C>A | XP_011519676.1:n.4093+2921C>A | |
| XM_011521375.3:c.4064-1459C>A | XP_011519677.1:n.4064-1459C>A | |
| XM_011521378.3:c.4063+2951C>A | XP_011519680.1:n.4063+2951C>A | |
| XM_011521379.3:c.*572C>A | XP_011519681.1:n.*572C>A | |
| XM_011521381.2:c.2737C>A | XP_011519683.1:p.Leu913Ile | |
| XM_017022015.1:c.2737C>A | XP_016877504.1:p.Leu913Ile | |
| XM_024449875.1:c.4504C>A | XP_024305643.1:p.Leu1502Ile | |
| XR_001751153.2:n.5014+2951C>A | ||
| XR_931769.3:n.5015-1459C>A | ||
| XR_931770.3:n.5044+2921C>A | ||
| XR_931775.3:n.5014+2951C>A | ||
| NM_001194998.2:c.4702C>A MANE Select | NP_001181927.1:p.Leu1568Ile | |
| NM_014985.4:c.4534C>A | NP_055800.2:p.Leu1512Ile |