HGVS | Genome Assembly |
---|---|
NC_000014.9:g.28768069G>A , CM000676.2:g.28768069G>A | GRCh38 |
NC_000014.8:g.29237275G>A , CM000676.1:g.29237275G>A | GRCh37 |
NC_000014.7:g.28307026G>A | NCBI36 |
NG_009367.1:g.5989G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000706482.1:c.790G>A | ENSP00000516406.1:p.Val264Met | |
ENST00000313071.7:c.790G>A MANE Select | ENSP00000339004.3:p.Val264Met | |
ENST00000313071.6:c.790G>A | ENSP00000339004.3:p.Val264Met | |
NM_005249.4:c.790G>A | NP_005240.3:p.Val264Met | |
NM_005249.5:c.790G>A MANE Select | NP_005240.3:p.Val264Met |