Linked Data
ClinVar Variation Id:
313801
ClinVar RCV Id:
RCV000313362
dbSNP Id:
rs1957949
gnomAD v2:
14-65542607-C-T
gnomAD v3:
14-65075889-C-T
gnomAD v4:
14-65075889-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.65075889C>T , CM000676.2:g.65075889C>T | GRCh38 |
| NC_000014.8:g.65542607C>T , CM000676.1:g.65542607C>T | GRCh37 |
| NC_000014.7:g.64612360C>T | NCBI36 |
| NG_029830.1:g.31621G>A , LRG_530:g.31621G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000556892.6:c.*587G>A | ENSP00000452206.2:n.*587G>A | |
| ENST00000556979.6:c.*1523G>A | ENSP00000452378.1:n.*1523G>A | |
| ENST00000358664.9:c.*587G>A MANE Select | ENSP00000351490.4:n.*587G>A | |
| ENST00000651648.1:c.145-5520G>A | ENSP00000498863.1:n.145-5520G>A | |
| ENST00000284165.10:c.*1914G>A | ENSP00000284165.6:n.*1914G>A | |
| ENST00000341653.6:c.171+17819G>A | ENSP00000342482.2:n.171+17819G>A | |
| ENST00000358402.8:c.*587G>A | ENSP00000351175.4:n.*587G>A | |
| ENST00000358664.8:c.*587G>A | ENSP00000351490.4:n.*587G>A | |
| ENST00000394606.6:c.*843G>A | ENSP00000378104.2:n.*843G>A | |
| ENST00000555932.5:c.*562G>A | ENSP00000450763.1:n.*562G>A | |
| ENST00000618858.4:c.*859G>A | ENSP00000480127.1:n.*859G>A | |
| NM_001271069.1:c.144+17819G>A | NP_001257998.1:n.144+17819G>A | |
| NM_002382.4:c.*587G>A | NP_002373.3:n.*587G>A | |
| NM_145112.2:c.*587G>A | NP_660087.1:n.*587G>A | |
| NM_145113.2:c.*859G>A | NP_660088.1:n.*859G>A | |
| NM_197957.3:c.171+17819G>A | NP_932061.1:n.171+17819G>A | |
| NR_073137.1:n.1194G>A | ||
| XR_429315.2:n.1357G>A | ||
| NM_001320415.1:c.*587G>A | NP_001307344.1:n.*587G>A | |
| XM_017021312.2:c.*587G>A | XP_016876801.1:n.*587G>A | |
| XM_017021313.1:c.*587G>A | XP_016876802.1:n.*587G>A | |
| XR_001750326.2:n.1415G>A | ||
| XR_001750327.2:n.1334G>A | ||
| XR_002957553.1:n.1848G>A | ||
| XR_943450.3:n.1438G>A | ||
| XR_943451.3:n.1454G>A | ||
| XR_943452.3:n.1399G>A | ||
| NM_001320415.2:c.*587G>A | NP_001307344.1:n.*587G>A | |
| NM_002382.5:c.*587G>A MANE Select | NP_002373.3:n.*587G>A | |
| NM_145112.3:c.*587G>A | NP_660087.1:n.*587G>A | |
| NM_145113.3:c.*859G>A | NP_660088.1:n.*859G>A | |
| NM_001271069.2:c.144+17819G>A | NP_001257998.1:n.144+17819G>A | |
| NM_197957.4:c.171+17819G>A | NP_932061.1:n.171+17819G>A |