Linked Data
ClinVar Variation Id:
427613
dbSNP Id:
rs786203847
COSMIC:
COSM86945
PubMed:
PMID:28677221
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.87925512G>C , CM000672.2:g.87925512G>C | GRCh38 |
| NC_000010.10:g.89685269G>C , CM000672.1:g.89685269G>C | GRCh37 |
| NC_000010.9:g.89675249G>C | NCBI36 |
| NG_007466.2:g.67074G>C , LRG_311:g.67074G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000700029.2:c.165-1G>C | ENSP00000514759.2:n.165-1G>C | |
| ENST00000710265.1:c.165-1G>C | ENSP00000518161.1:n.165-1G>C | |
| ENST00000472832.3:c.165-1G>C | ENSP00000483066.2:n.165-1G>C | |
| ENST00000688158.2:n.900-1G>C | ||
| ENST00000688922.2:c.165-1G>C | ENSP00000508742.2:n.165-1G>C | |
| ENST00000700021.1:c.165-5534G>C | ENSP00000514757.1:n.165-5534G>C | |
| ENST00000700022.1:c.165-1G>C | ENSP00000514758.1:n.165-1G>C | |
| ENST00000706954.1:c.165-1G>C | ENSP00000516674.1:n.165-1G>C | |
| ENST00000706955.1:c.*200-1G>C | ENSP00000516675.1:n.*200-1G>C | |
| ENST00000686459.1:c.165-1G>C | ENSP00000508909.1:n.165-1G>C | |
| ENST00000688158.1:c.*276-1G>C | ENSP00000509254.1:n.*276-1G>C | |
| ENST00000688308.1:c.165-1G>C | ENSP00000508752.1:n.165-1G>C | |
| ENST00000688922.1:c.34-1G>C | ||
| ENST00000693560.1:c.684-1G>C | ENSP00000509861.1:n.684-1G>C | |
| ENST00000371953.8:c.165-1G>C MANE Select | ENSP00000361021.3:n.165-1G>C | |
| ENST00000371953.7:c.165-1G>C | ENSP00000361021.3:n.165-1G>C | |
| ENST00000610634.1:c.63-1G>C | ENSP00000477517.1:n.63-1G>C | |
| NM_000314.5:c.165-1G>C | NP_000305.3:n.165-1G>C | |
| NM_000314.6:c.165-1G>C | NP_000305.3:n.165-1G>C | |
| NM_001304717.2:c.684-1G>C | NP_001291646.2:n.684-1G>C | |
| NM_001304718.1:c.-541-5534G>C | NP_001291647.1:n.-541-5534G>C | |
| XM_006717926.2:c.165-5534G>C | XP_006717989.1:n.165-5534G>C | |
| XM_011539981.1:c.165-1G>C | XP_011538283.1:n.165-1G>C | |
| XM_011539982.1:c.69-1G>C | XP_011538284.1:n.69-1G>C | |
| XR_945789.1:n.877-1G>C | ||
| XR_945790.1:n.877-1G>C | ||
| XR_945791.1:n.877-1G>C | ||
| NM_000314.7:c.165-1G>C | NP_000305.3:n.165-1G>C | |
| NM_001304717.5:c.684-1G>C | NP_001291646.4:n.684-1G>C | |
| NM_001304718.2:c.-541-5534G>C | NP_001291647.1:n.-541-5534G>C | |
| NM_000314.8:c.165-1G>C MANE Select | NP_000305.3:n.165-1G>C |