HGVS | Genome Assembly |
---|---|
NC_000002.12:g.96265279G>C , CM000664.2:g.96265279G>C | GRCh38 |
NC_000002.11:g.96931017G>C , CM000664.1:g.96931017G>C | GRCh37 |
NC_000002.10:g.96294744G>C | NCBI36 |
NG_027695.1:g.5735C>G , LRG_528:g.5735C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000258439.8:c.103C>G MANE Select | ENSP00000258439.3:p.Leu35Val | |
ENST00000258439.7:c.103C>G | ENSP00000258439.2:p.Leu35Val | |
ENST00000432959.1:c.103C>G | ENSP00000416660.1:p.Leu35Val | |
NM_001193304.2:c.103C>G | NP_001180233.1:p.Leu35Val | |
NM_017849.3:c.103C>G , LRG_528t1:c.103C>G | NP_060319.1:p.Leu35Val | |
NM_001193304.3:c.103C>G | NP_001180233.1:p.Leu35Val | |
NM_017849.4:c.103C>G MANE Select | NP_060319.1:p.Leu35Val |