HGVS | Genome Assembly |
---|---|
NC_000005.10:g.177992937A= , CM000667.2:g.177992937A= | GRCh38 |
NC_000005.9:g.177419938A= , CM000667.1:g.177419938A= | GRCh37 |
NC_000005.8:g.177352544A= | NCBI36 |
NG_015889.1:g.8306T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000308304.2:c.453T= MANE Select | ENSP00000311290.2:p.Thr151= | |
NM_006261.4:c.453T= | NP_006252.3:p.Thr151= | |
NM_006261.5:c.453T= MANE Select | NP_006252.4:p.Thr151= |