HGVS | Genome Assembly |
---|---|
NC_000002.12:g.166196565T= , CM000664.2:g.166196565T= | GRCh38 |
NC_000002.11:g.167053075T= , CM000664.1:g.167053075T= | GRCh37 |
NC_000002.10:g.166761321T= | NCBI36 |
NG_012798.1:g.184423A= , LRG_369:g.184423A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000303354.11:c.*2107A= (SCN9A) | ENSP00000304748.7:n.*2107A= | |
ENST00000642356.2:c.*2107A= (SCN9A) MANE Select | ENSP00000495601.1:n.*2107A= | |
ENST00000303354.10:c.*2107A= (SCN9A) | ENSP00000304748.7:n.*2107A= | |
ENST00000409672.5:c.*2107A= (SCN9A) | ENSP00000386306.1:n.*2107A= | |
NM_002977.3:c.*2107A= , LRG_369t1:c.*2107A= (SCN9A) | NP_002968.1:n.*2107A= | |
NR_110260.1:n.432-3074T= (SCN1A-AS1) | ||
NM_001365536.1:c.*2107A= (SCN9A) MANE Select | NP_001352465.1:n.*2107A= |