HGVS | Genome Assembly |
---|---|
NC_000004.12:g.46085761A= , CM000666.2:g.46085761A= | GRCh38 |
NC_000004.11:g.46087778A= , CM000666.1:g.46087778A= | GRCh37 |
NC_000004.10:g.45782535A= | NCBI36 |
NG_046964.1:g.43305T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000295452.5:c.254-1708T= MANE Select | ENSP00000295452.4:n.254-1708T= | |
ENST00000295452.4:c.254-1708T= | ENSP00000295452.4:n.254-1708T= | |
NM_173536.3:c.254-1708T= | NP_775807.2:n.254-1708T= | |
NM_173536.4:c.254-1708T= MANE Select | NP_775807.2:n.254-1708T= |