HGVS | Genome Assembly |
---|---|
NC_000014.9:g.28767564C>G , CM000676.2:g.28767564C>G | GRCh38 |
NC_000014.8:g.29236770C>G , CM000676.1:g.29236770C>G | GRCh37 |
NC_000014.7:g.28306521C>G | NCBI36 |
NG_009367.1:g.5484C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000706482.1:c.285C>G | ENSP00000516406.1:p.Asp95Glu | |
ENST00000313071.7:c.285C>G MANE Select | ENSP00000339004.3:p.Asp95Glu | |
ENST00000313071.6:c.285C>G | ENSP00000339004.3:p.Asp95Glu | |
NM_005249.4:c.285C>G | NP_005240.3:p.Asp95Glu | |
NM_005249.5:c.285C>G MANE Select | NP_005240.3:p.Asp95Glu |