HGVS | Genome Assembly |
---|---|
NC_000023.11:g.50915784T= , CM000685.2:g.50915784T= | GRCh38 |
NC_000023.10:g.50658784T= , CM000685.1:g.50658784T= | GRCh37 |
NC_000023.9:g.50675524T= | NCBI36 |
NG_012894.1:g.10001T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000252677.4:c.356T= MANE Select | ENSP00000252677.3:p.Phe119= | |
ENST00000252677.3:c.356T= | ENSP00000252677.3:p.Phe119= | |
NM_005448.2:c.356T= MANE Select | NP_005439.2:p.Phe119= |