HGVS | Genome Assembly |
---|---|
NC_000011.10:g.640283T>G , CM000673.2:g.640283T>G | GRCh38 |
NC_000011.9:g.640283T>G , CM000673.1:g.640283T>G | GRCh37 |
NC_000011.8:g.630283T>G | NCBI36 |
NG_021241.1:g.7979T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000176183.6:c.1034T>G MANE Select | ENSP00000176183.5:p.Met345Arg | |
ENST00000176183.5:c.1034T>G | ENSP00000176183.5:p.Met345Arg | |
NM_000797.3:c.1034T>G | NP_000788.2:p.Met345Arg | |
NM_000797.4:c.1034T>G MANE Select | NP_000788.2:p.Met345Arg |