HGVS | Genome Assembly |
---|---|
NC_000001.11:g.55053145A= , CM000663.2:g.55053145A= | GRCh38 |
NC_000001.10:g.55518818A= , CM000663.1:g.55518818A= | GRCh37 |
NC_000001.9:g.55291406A= | NCBI36 |
NG_009061.1:g.18599A= , LRG_275:g.18599A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000673913.2:c.799+354A= | ENSP00000501161.2:n.799+354A= | |
ENST00000710286.1:c.1156+354A= | ENSP00000518176.1:n.1156+354A= | |
ENST00000673903.1:c.424+354A= | ENSP00000501257.1:n.424+354A= | |
ENST00000302118.5:c.799+354A= MANE Select | ENSP00000303208.5:n.799+354A= | |
ENST00000490692.1:n.1620+354A= | ||
NM_174936.3:c.799+354A= , LRG_275t1:c.799+354A= | NP_777596.2:n.799+354A= | |
NR_110451.1:n.458+354A= | ||
NM_174936.4:c.799+354A= MANE Select | NP_777596.2:n.799+354A= | |
NR_110451.2:n.458+354A= |