HGVS | Genome Assembly |
---|---|
NC_000012.12:g.52519911C= , CM000674.2:g.52519911C= | GRCh38 |
NC_000012.11:g.52913695C= , CM000674.1:g.52913695C= | GRCh37 |
NC_000012.10:g.51199962C= | NCBI36 |
NG_008297.1:g.5549G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000252242.9:c.386G= MANE Select | ENSP00000252242.4:p.Gly129= | |
ENST00000252242.8:c.386G= | ENSP00000252242.4:p.Gly129= | |
ENST00000546577.1:c.386G= | ENSP00000449651.1:p.Gly129= | |
ENST00000549420.1:c.56G= | ENSP00000447209.1:p.Gly19= | |
ENST00000551275.1:c.281G= | ENSP00000448041.1:p.Gly94= | |
ENST00000552629.5:n.484G= | ||
NM_000424.3:c.386G= | NP_000415.2:p.Gly129= | |
NM_000424.4:c.386G= MANE Select | NP_000415.2:p.Gly129= |