HGVS | Genome Assembly |
---|---|
NC_000021.9:g.43774212G>C , CM000683.2:g.43774212G>C | GRCh38 |
NC_000021.8:g.45194093G>C , CM000683.1:g.45194093G>C | GRCh37 |
NC_000021.7:g.44018521G>C | NCBI36 |
NG_011545.1:g.7167C>G , LRG_485:g.7167C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000291568.7:c.287C>G MANE Select | ENSP00000291568.6:p.Thr96Ser | |
ENST00000480147.3:n.2057C>G | ||
ENST00000639959.1:c.154C>G | ||
ENST00000640406.1:c.*362C>G | ENSP00000492672.1:n.*362C>G | |
ENST00000675996.1:n.712C>G | ||
ENST00000291568.5:c.287C>G | ENSP00000291568.5:p.Thr96Ser | |
ENST00000480147.1:n.651C>G | ||
NM_000100.3:c.287C>G , LRG_485t1:c.287C>G | NP_000091.1:p.Thr96Ser | |
NM_000100.4:c.287C>G MANE Select | NP_000091.1:p.Thr96Ser |