HGVS | Genome Assembly |
---|---|
NC_000001.11:g.55052312C= , CM000663.2:g.55052312C= | GRCh38 |
NC_000001.10:g.55517985C= , CM000663.1:g.55517985C= | GRCh37 |
NC_000001.9:g.55290573C= | NCBI36 |
NG_009061.1:g.17766C= , LRG_275:g.17766C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000673913.2:c.558C= | ENSP00000501161.2:p.Asp186= | |
ENST00000710286.1:c.915C= | ENSP00000518176.1:p.Asp305= | |
ENST00000673726.1:c.*54C= | ENSP00000501004.1:n.*54C= | |
ENST00000673903.1:c.183C= | ENSP00000501257.1:p.Asp61= | |
ENST00000302118.5:c.558C= MANE Select | ENSP00000303208.5:p.Asp186= | |
ENST00000490692.1:n.1379C= | ||
NM_174936.3:c.558C= , LRG_275t1:c.558C= | NP_777596.2:p.Asp186= | |
NR_110451.1:n.217C= | ||
NM_174936.4:c.558C= MANE Select | NP_777596.2:p.Asp186= | |
NR_110451.2:n.217C= |