HGVS | Genome Assembly |
---|---|
NC_000002.12:g.96265164C>A , CM000664.2:g.96265164C>A | GRCh38 |
NC_000002.11:g.96930902C>A , CM000664.1:g.96930902C>A | GRCh37 |
NC_000002.10:g.96294629C>A | NCBI36 |
NG_027695.1:g.5850G>T , LRG_528:g.5850G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000258439.8:c.218G>T MANE Select | ENSP00000258439.3:p.Gly73Val | |
ENST00000258439.7:c.218G>T | ENSP00000258439.2:p.Gly73Val | |
ENST00000432959.1:c.218G>T | ENSP00000416660.1:p.Gly73Val | |
NM_001193304.2:c.218G>T | NP_001180233.1:p.Gly73Val | |
NM_017849.3:c.218G>T , LRG_528t1:c.218G>T | NP_060319.1:p.Gly73Val | |
NM_001193304.3:c.218G>T | NP_001180233.1:p.Gly73Val | |
NM_017849.4:c.218G>T MANE Select | NP_060319.1:p.Gly73Val |