Linked Data
ClinVar Variation Id:
2823851
ClinVar RCV Id:
RCV003651017
dbSNP Id:
rs762797471
ExAC:
7:55248977 T / G
gnomAD v2:
7-55248977-T-G
gnomAD v3:
7-55181284-T-G
gnomAD v4:
7-55181284-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.55181284T>G , CM000669.2:g.55181284T>G | GRCh38 |
| NC_000007.13:g.55248977T>G , CM000669.1:g.55248977T>G | GRCh37 |
| NC_000007.12:g.55216471T>G | NCBI36 |
| NG_007726.3:g.167253T>G , LRG_304:g.167253T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000450046.2:c.2125-9T>G (EGFR) | ENSP00000413354.2:n.2125-9T>G | |
| ENST00000700145.1:c.633-9T>G (EGFR) | ||
| ENST00000275493.7:c.2284-9T>G (EGFR) MANE Select | ENSP00000275493.2:n.2284-9T>G | |
| ENST00000275493.6:c.2284-9T>G (EGFR) | ENSP00000275493.2:n.2284-9T>G | |
| ENST00000442591.5:c.*28+8356T>G (EGFR) | ENSP00000410031.1:n.*28+8356T>G | |
| ENST00000454757.6:c.2149-9T>G (EGFR) | ENSP00000395243.3:n.2149-9T>G | |
| ENST00000455089.5:c.2149-9T>G (EGFR) | ENSP00000415559.1:n.2149-9T>G | |
| NM_005228.3:c.2284-9T>G , LRG_304t1:c.2284-9T>G (EGFR) | NP_005219.2:n.2284-9T>G | |
| NR_047551.1:n.1287A>C (EGFR-AS1) | ||
| NM_001346897.1:c.2149-9T>G (EGFR) | NP_001333826.1:n.2149-9T>G | |
| NM_001346898.1:c.2284-9T>G (EGFR) | NP_001333827.1:n.2284-9T>G | |
| NM_001346899.1:c.2149-9T>G (EGFR) | NP_001333828.1:n.2149-9T>G | |
| NM_001346900.1:c.2125-9T>G (EGFR) | NP_001333829.1:n.2125-9T>G | |
| NM_001346941.1:c.1483-9T>G (EGFR) | NP_001333870.1:n.1483-9T>G | |
| NM_005228.4:c.2284-9T>G (EGFR) | NP_005219.2:n.2284-9T>G | |
| NM_005228.5:c.2284-9T>G (EGFR) MANE Select | NP_005219.2:n.2284-9T>G | |
| NM_001346897.2:c.2149-9T>G (EGFR) | NP_001333826.1:n.2149-9T>G | |
| NM_001346898.2:c.2284-9T>G (EGFR) | NP_001333827.1:n.2284-9T>G | |
| NM_001346900.2:c.2125-9T>G (EGFR) | NP_001333829.1:n.2125-9T>G | |
| NM_001346941.2:c.1483-9T>G (EGFR) | NP_001333870.1:n.1483-9T>G | |
| NM_001346899.2:c.2149-9T>G (EGFR) | NP_001333828.1:n.2149-9T>G |