HGVS | Genome Assembly |
---|---|
NC_000018.10:g.31595179G>T , CM000680.2:g.31595179G>T | GRCh38 |
NC_000018.9:g.29175142G>T , CM000680.1:g.29175142G>T | GRCh37 |
NC_000018.8:g.27429140G>T | NCBI36 |
NG_009490.1:g.8413G>T , LRG_416:g.8413G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000237014.8:c.260G>T MANE Select | ENSP00000237014.4:p.Gly87Val | |
ENST00000610404.5:c.164G>T | ENSP00000477599.2:p.Gly55Val | |
ENST00000649620.1:c.260G>T | ENSP00000497927.1:p.Gly87Val | |
ENST00000237014.7:c.260G>T | ENSP00000237014.3:p.Gly87Val | |
ENST00000541025.2:n.286G>T | ||
ENST00000610404.4:c.260G>T | ENSP00000477599.1:p.Gly87Val | |
ENST00000613781.1:c.260G>T | ENSP00000479174.1:p.Gly87Val | |
NM_000371.3:c.260G>T , LRG_416t1:c.260G>T | NP_000362.1:p.Gly87Val | |
NM_000371.4:c.260G>T MANE Select | NP_000362.1:p.Gly87Val |