HGVS | Genome Assembly |
---|---|
NC_000022.11:g.20242776C= , CM000684.2:g.20242776C= | GRCh38 |
NC_000022.10:g.20230299C= , CM000684.1:g.20230299C= | GRCh37 |
NC_000022.9:g.18610299C= | NCBI36 |
NG_012176.1:g.30518G= | |
NG_012176.2:g.30518G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000043402.8:c.357G= MANE Select | ENSP00000043402.7:p.Arg119= | |
ENST00000043402.7:c.357G= | ENSP00000043402.7:p.Arg119= | |
ENST00000416372.5:c.416G= | ||
ENST00000425986.1:c.614G= | ||
ENST00000469601.1:n.493G= | ||
NM_023004.5:c.357G= | NP_075380.1:p.Arg119= | |
NM_023004.6:c.357G= MANE Select | NP_075380.1:p.Arg119= |