HGVS | Genome Assembly |
---|---|
NC_000018.10:g.31598737T>A , CM000680.2:g.31598737T>A | GRCh38 |
NC_000018.9:g.29178700T>A , CM000680.1:g.29178700T>A | GRCh37 |
NC_000018.8:g.27432698T>A | NCBI36 |
NG_009490.1:g.11971T>A , LRG_416:g.11971T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000237014.8:c.*62T>A MANE Select | ENSP00000237014.4:n.*62T>A | |
ENST00000610404.5:c.*62T>A | ENSP00000477599.2:n.*62T>A | |
ENST00000649620.1:c.*62T>A | ENSP00000497927.1:n.*62T>A | |
ENST00000237014.7:c.*62T>A | ENSP00000237014.3:n.*62T>A | |
ENST00000610404.4:c.*62T>A | ENSP00000477599.1:n.*62T>A | |
NM_000371.3:c.*62T>A , LRG_416t1:c.*62T>A | NP_000362.1:n.*62T>A | |
NM_000371.4:c.*62T>A MANE Select | NP_000362.1:n.*62T>A |