HGVS | Genome Assembly |
---|---|
NC_000008.11:g.6870608T= , CM000670.2:g.6870608T= | GRCh38 |
NC_000008.10:g.6728130T= , CM000670.1:g.6728130T= | GRCh37 |
NC_000008.9:g.6715540T= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000297439.4:c.*73A= MANE Select | ENSP00000297439.3:n.*73A= | |
ENST00000297439.3:c.*73A= | ENSP00000297439.3:n.*73A= | |
NM_005218.3:c.*73A= | NP_005209.1:n.*73A= | |
NM_005218.4:c.*73A= MANE Select | NP_005209.1:n.*73A= |