HGVS | Genome Assembly |
---|---|
NC_000016.10:g.177000T>A , CM000678.2:g.177000T>A | GRCh38 |
NC_000016.9:g.226999T>A , CM000678.1:g.226999T>A | GRCh37 |
NC_000016.8:g.166999T>A | NCBI36 |
NG_000006.1:g.37863T>A | |
NG_059186.1:g.5350T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000320868.9:c.167T>A MANE Select | ENSP00000322421.5:p.Val56Asp | |
ENST00000397797.1:c.71T>A | ENSP00000380899.1:p.Val24Asp | |
ENST00000472694.1:n.303T>A | ||
ENST00000487791.1:n.136T>A | ||
NM_000558.4:c.167T>A | NP_000549.1:p.Val56Asp | |
NM_000558.5:c.167T>A MANE Select | NP_000549.1:p.Val56Asp |