HGVS | Genome Assembly |
---|---|
NC_000007.14:g.55183900A>G , CM000669.2:g.55183900A>G | GRCh38 |
NC_000007.13:g.55251593A>G , CM000669.1:g.55251593A>G | GRCh37 |
NC_000007.12:g.55219087A>G | NCBI36 |
NG_007726.3:g.169869A>G , LRG_304:g.169869A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000450046.2:c.2310+2422A>G (EGFR) | ENSP00000413354.2:n.2310+2422A>G | |
ENST00000700145.1:c.818+2422A>G (EGFR) | ||
ENST00000275493.7:c.2469+2422A>G (EGFR) MANE Select | ENSP00000275493.2:n.2469+2422A>G | |
ENST00000275493.6:c.2469+2422A>G (EGFR) | ENSP00000275493.2:n.2469+2422A>G | |
ENST00000442591.5:c.*28+10972A>G (EGFR) | ENSP00000410031.1:n.*28+10972A>G | |
ENST00000454757.6:c.2334+2422A>G (EGFR) | ENSP00000395243.3:n.2334+2422A>G | |
ENST00000455089.5:c.2334+2422A>G (EGFR) | ENSP00000415559.1:n.2334+2422A>G | |
NM_005228.3:c.2469+2422A>G , LRG_304t1:c.2469+2422A>G (EGFR) | NP_005219.2:n.2469+2422A>G | |
NR_047551.1:n.94-1423T>C (EGFR-AS1) | ||
NM_001346897.1:c.2334+2422A>G (EGFR) | NP_001333826.1:n.2334+2422A>G | |
NM_001346898.1:c.2469+2422A>G (EGFR) | NP_001333827.1:n.2469+2422A>G | |
NM_001346899.1:c.2334+2422A>G (EGFR) | NP_001333828.1:n.2334+2422A>G | |
NM_001346900.1:c.2310+2422A>G (EGFR) | NP_001333829.1:n.2310+2422A>G | |
NM_001346941.1:c.1668+2422A>G (EGFR) | NP_001333870.1:n.1668+2422A>G | |
NM_005228.4:c.2469+2422A>G (EGFR) | NP_005219.2:n.2469+2422A>G | |
NM_005228.5:c.2469+2422A>G (EGFR) MANE Select | NP_005219.2:n.2469+2422A>G | |
NM_001346897.2:c.2334+2422A>G (EGFR) | NP_001333826.1:n.2334+2422A>G | |
NM_001346898.2:c.2469+2422A>G (EGFR) | NP_001333827.1:n.2469+2422A>G | |
NM_001346900.2:c.2310+2422A>G (EGFR) | NP_001333829.1:n.2310+2422A>G | |
NM_001346941.2:c.1668+2422A>G (EGFR) | NP_001333870.1:n.1668+2422A>G | |
NM_001346899.2:c.2334+2422A>G (EGFR) | NP_001333828.1:n.2334+2422A>G |