Linked Data
ClinVar Variation Id:
314485
ClinVar RCV Id:
RCV000376138
dbSNP Id:
rs765906060
ExAC:
14:76929019 C / T
gnomAD v2:
14-76929019-C-T
gnomAD v3:
14-76462676-C-T
gnomAD v4:
14-76462676-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.76462676C>T , CM000676.2:g.76462676C>T | GRCh38 |
| NC_000014.8:g.76929019C>T , CM000676.1:g.76929019C>T | GRCh37 |
| NC_000014.7:g.75998772C>T | NCBI36 |
| NG_012278.1:g.96330C>T | |
| NG_012278.2:g.96330C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000380887.7:c.514+15C>T | ENSP00000370270.2:n.514+15C>T | |
| ENST00000505752.6:c.514+15C>T | ENSP00000423004.1:n.514+15C>T | |
| ENST00000512784.6:c.529+15C>T | ENSP00000424992.2:n.529+15C>T | |
| ENST00000644823.1:c.577+15C>T MANE Select | ENSP00000493776.1:n.577+15C>T | |
| ENST00000380887.6:c.514+15C>T | ENSP00000370270.2:n.514+15C>T | |
| ENST00000505752.5:c.514+15C>T | ENSP00000423004.1:n.514+15C>T | |
| ENST00000507951.5:n.622+15C>T | ||
| ENST00000509242.5:c.514+15C>T | ENSP00000422488.1:n.514+15C>T | |
| ENST00000509323.1:n.226+15C>T | ||
| ENST00000512784.5:c.529+15C>T | ENSP00000424992.1:n.529+15C>T | |
| ENST00000556177.1:c.514+15C>T | ENSP00000451658.1:n.514+15C>T | |
| NM_004452.3:c.514+15C>T | NP_004443.3:n.514+15C>T | |
| XM_005267404.2:c.577+15C>T | XP_005267461.1:n.577+15C>T | |
| XM_011536547.1:c.577+15C>T | XP_011534849.1:n.577+15C>T | |
| XM_011536548.1:c.514+15C>T | XP_011534850.1:n.514+15C>T | |
| XM_011536549.1:c.514+15C>T | XP_011534851.1:n.514+15C>T | |
| XM_011536550.1:c.514+15C>T | XP_011534852.1:n.514+15C>T | |
| XM_011536551.1:c.514+15C>T | XP_011534853.1:n.514+15C>T | |
| XM_011536552.1:c.514+15C>T | XP_011534854.1:n.514+15C>T | |
| XM_011536553.1:c.577+15C>T | XP_011534855.1:n.577+15C>T | |
| XM_011536554.1:c.577+15C>T | XP_011534856.1:n.577+15C>T | |
| XR_943401.1:n.824+15C>T | ||
| XM_011536547.2:c.577+15C>T | XP_011534849.1:n.577+15C>T | |
| XM_011536550.2:c.514+15C>T | XP_011534852.1:n.514+15C>T | |
| XM_011536553.2:c.577+15C>T | XP_011534855.1:n.577+15C>T | |
| XM_011536554.2:c.577+15C>T | XP_011534856.1:n.577+15C>T | |
| XM_017021085.1:c.514+15C>T | XP_016876574.1:n.514+15C>T | |
| XM_024449508.1:c.577+15C>T | XP_024305276.1:n.577+15C>T | |
| XM_024449509.1:c.514+15C>T | XP_024305277.1:n.514+15C>T | |
| XR_001750189.1:n.1047+15C>T | ||
| XR_943401.2:n.1047+15C>T | ||
| NM_001379180.1:c.577+15C>T MANE Select | NP_001366109.1:n.577+15C>T | |
| NM_004452.4:c.514+15C>T | NP_004443.3:n.514+15C>T |