HGVS | Genome Assembly |
---|---|
NC_000001.11:g.204165335A= , CM000663.2:g.204165335A= | GRCh38 |
NC_000001.10:g.204134463A= , CM000663.1:g.204134463A= | GRCh37 |
NC_000001.9:g.202401086A= | NCBI36 |
NG_012122.1:g.6003T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000272190.9:c.98+861T= MANE Select | ENSP00000272190.8:n.98+861T= | |
ENST00000638118.1:c.-16-3172T= | ENSP00000490307.1:n.-16-3172T= | |
ENST00000272190.8:c.98+861T= | ENSP00000272190.8:n.98+861T= | |
NM_000537.3:c.98+861T= | NP_000528.1:n.98+861T= | |
NM_000537.4:c.98+861T= MANE Select | NP_000528.1:n.98+861T= |