HGVS | Genome Assembly |
---|---|
NC_000015.10:g.74749933G>A , CM000677.2:g.74749933G>A | GRCh38 |
NC_000015.9:g.75042274G>A , CM000677.1:g.75042274G>A | GRCh37 |
NC_000015.8:g.72829327G>A | NCBI36 |
NG_008431.1:g.32392G>A | |
NG_008431.2:g.32392G>A | |
NG_061543.1:g.6089G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000343932.5:c.195G>A MANE Select | ENSP00000342007.4:p.Leu65= | |
ENST00000343932.4:c.195G>A | ENSP00000342007.4:p.Leu65= | |
NM_000761.4:c.195G>A | NP_000752.2:p.Leu65= | |
NM_000761.5:c.195G>A MANE Select | NP_000752.2:p.Leu65= |