HGVS | Genome Assembly |
---|---|
NC_000001.11:g.55052770A= , CM000663.2:g.55052770A= | GRCh38 |
NC_000001.10:g.55518443A= , CM000663.1:g.55518443A= | GRCh37 |
NC_000001.9:g.55291031A= | NCBI36 |
NG_009061.1:g.18224A= , LRG_275:g.18224A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000673913.2:c.778A= | ENSP00000501161.2:p.Thr260= | |
ENST00000710286.1:c.1135A= | ENSP00000518176.1:p.Thr379= | |
ENST00000673903.1:c.403A= | ENSP00000501257.1:p.Thr135= | |
ENST00000302118.5:c.778A= MANE Select | ENSP00000303208.5:p.Thr260= | |
ENST00000490692.1:n.1599A= | ||
NM_174936.3:c.778A= , LRG_275t1:c.778A= | NP_777596.2:p.Thr260= | |
NR_110451.1:n.437A= | ||
NM_174936.4:c.778A= MANE Select | NP_777596.2:p.Thr260= | |
NR_110451.2:n.437A= |