HGVS | Genome Assembly |
---|---|
NC_000023.11:g.78113894G>A , CM000685.2:g.78113894G>A | GRCh38 |
NC_000023.10:g.77369391G>A , CM000685.1:g.77369391G>A | GRCh37 |
NC_000023.9:g.77256047G>A | NCBI36 |
NG_008862.1:g.14726G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000373316.5:c.267G>A MANE Select | ENSP00000362413.4:p.Leu89= | |
ENST00000644362.1:c.183G>A | ENSP00000496140.1:p.Leu61= | |
ENST00000373316.4:c.267G>A | ENSP00000362413.4:p.Leu89= | |
ENST00000491291.1:n.259G>A | ||
NM_000291.3:c.267G>A | NP_000282.1:p.Leu89= | |
NM_000291.4:c.267G>A MANE Select | NP_000282.1:p.Leu89= |