HGVS | Genome Assembly |
---|---|
NC_000023.11:g.78118116A>T , CM000685.2:g.78118116A>T | GRCh38 |
NC_000023.10:g.77373613A>T , CM000685.1:g.77373613A>T | GRCh37 |
NC_000023.9:g.77260269A>T | NCBI36 |
NG_008862.1:g.18948A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000373316.5:c.587A>T MANE Select | ENSP00000362413.4:p.Tyr196Phe | |
ENST00000644362.1:c.503A>T | ENSP00000496140.1:p.Tyr168Phe | |
ENST00000373316.4:c.587A>T | ENSP00000362413.4:p.Tyr196Phe | |
ENST00000491291.1:n.579A>T | ||
NM_000291.3:c.587A>T | NP_000282.1:p.Tyr196Phe | |
NM_000291.4:c.587A>T MANE Select | NP_000282.1:p.Tyr196Phe |