Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.166195650C= , CM000664.2:g.166195650C= | GRCh38 |
| NC_000002.11:g.167052160C= , CM000664.1:g.167052160C= | GRCh37 |
| NC_000002.10:g.166760406C= | NCBI36 |
| NG_012798.1:g.185338G= , LRG_369:g.185338G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000303354.11:c.*3022G= (SCN9A) | ENSP00000304748.7:n.*3022G= | |
| ENST00000642356.2:c.*3022G= (SCN9A) MANE Select | ENSP00000495601.1:n.*3022G= | |
| ENST00000303354.10:c.*3022G= (SCN9A) | ENSP00000304748.7:n.*3022G= | |
| ENST00000409672.5:c.*3022G= (SCN9A) | ENSP00000386306.1:n.*3022G= | |
| NM_002977.3:c.*3022G= , LRG_369t1:c.*3022G= (SCN9A) | NP_002968.1:n.*3022G= | |
| NR_110260.1:n.432-3989C= (SCN1A-AS1) | ||
| NM_001365536.1:c.*3022G= (SCN9A) MANE Select | NP_001352465.1:n.*3022G= |