HGVS | Genome Assembly |
---|---|
NC_000002.12:g.166195888A>G , CM000664.2:g.166195888A>G | GRCh38 |
NC_000002.11:g.167052398A>G , CM000664.1:g.167052398A>G | GRCh37 |
NC_000002.10:g.166760644A>G | NCBI36 |
NG_012798.1:g.185100T>C , LRG_369:g.185100T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000303354.11:c.*2784T>C (SCN9A) | ENSP00000304748.7:n.*2784T>C | |
ENST00000642356.2:c.*2784T>C (SCN9A) MANE Select | ENSP00000495601.1:n.*2784T>C | |
ENST00000303354.10:c.*2784T>C (SCN9A) | ENSP00000304748.7:n.*2784T>C | |
ENST00000409672.5:c.*2784T>C (SCN9A) | ENSP00000386306.1:n.*2784T>C | |
NM_002977.3:c.*2784T>C , LRG_369t1:c.*2784T>C (SCN9A) | NP_002968.1:n.*2784T>C | |
NR_110260.1:n.432-3751A>G (SCN1A-AS1) | ||
NM_001365536.1:c.*2784T>C (SCN9A) MANE Select | NP_001352465.1:n.*2784T>C |