HGVS | Genome Assembly |
---|---|
NC_000004.12:g.186196961C>A , CM000666.2:g.186196961C>A | GRCh38 |
NC_000004.11:g.187118115C>A , CM000666.1:g.187118115C>A | GRCh37 |
NC_000004.10:g.187355109C>A | NCBI36 |
NG_007965.1:g.10442C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378802.5:c.435C>A MANE Select | ENSP00000368079.4:p.Ser145= | |
ENST00000378802.4:c.435C>A | ENSP00000368079.4:p.Ser145= | |
ENST00000507209.5:n.874C>A | ||
NM_207352.3:c.435C>A | NP_997235.3:p.Ser145= | |
XM_005262935.2:c.435C>A | XP_005262992.1:p.Ser145= | |
XM_006714184.2:c.39C>A | XP_006714247.1:p.Ser13= | |
XM_005262935.4:c.435C>A | XP_005262992.1:p.Ser145= | |
XM_017008037.1:c.39C>A | XP_016863526.1:p.Ser13= | |
NM_207352.4:c.435C>A MANE Select | NP_997235.3:p.Ser145= |