HGVS | Genome Assembly |
---|---|
NC_000023.11:g.136659110C>T , CM000685.2:g.136659110C>T | GRCh38 |
NC_000023.10:g.135741269C>T , CM000685.1:g.135741269C>T | GRCh37 |
NC_000023.9:g.135568935C>T | NCBI36 |
NG_007280.1:g.15934C>T , LRG_141:g.15934C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000695724.1:c.*99C>T | ENSP00000512122.1:n.*99C>T | |
ENST00000695725.1:c.*36C>T | ENSP00000512123.1:n.*36C>T | |
ENST00000695726.1:n.2449C>T | ||
ENST00000695729.1:n.3284C>T | ||
ENST00000370629.7:c.481C>T MANE Select | ENSP00000359663.2:p.Leu161= | |
ENST00000370628.2:c.418C>T | ENSP00000359662.2:p.Leu140= | |
ENST00000370629.6:c.481C>T | ENSP00000359663.2:p.Leu161= | |
NM_000074.2:c.481C>T , LRG_141t1:c.481C>T | NP_000065.1:p.Leu161= | |
NM_000074.3:c.481C>T MANE Select | NP_000065.1:p.Leu161= |