HGVS | Genome Assembly |
---|---|
NC_000008.11:g.86575902C= , CM000670.2:g.86575902C= | GRCh38 |
NC_000008.10:g.87588130C= , CM000670.1:g.87588130C= | GRCh37 |
NC_000008.9:g.87657246C= | NCBI36 |
NG_016980.1:g.172774G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000320005.6:c.2332G= MANE Select | ENSP00000316605.5:p.Gly778= | |
ENST00000681546.1:n.2152G= | ||
ENST00000681746.1:c.*743G= | ENSP00000505959.1:n.*743G= | |
ENST00000320005.5:c.2332G= | ENSP00000316605.5:p.Gly778= | |
ENST00000517327.5:c.276+2787G= | ENSP00000428329.1:n.276+2787G= | |
NM_019098.4:c.2332G= | NP_061971.3:p.Gly778= | |
XM_011517138.1:c.1918G= | XP_011515440.1:p.Gly640= | |
XM_011517138.2:c.1918G= | XP_011515440.1:p.Gly640= | |
NM_019098.5:c.2332G= MANE Select | NP_061971.3:p.Gly778= |