HGVS | Genome Assembly |
---|---|
NC_000010.11:g.110589894A= , CM000672.2:g.110589894A= | GRCh38 |
NC_000010.10:g.112349652A= , CM000672.1:g.112349652A= | GRCh37 |
NC_000010.9:g.112339642A= | NCBI36 |
NG_012217.1:g.27204A= , LRG_774:g.27204A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000684797.1:n.1312A= | ||
ENST00000684988.1:n.2057A= | ||
ENST00000687823.1:n.1326A= | ||
ENST00000689932.1:n.3475A= | ||
ENST00000691297.1:n.1545A= | ||
ENST00000691527.1:n.2215A= | ||
ENST00000692792.1:n.1531A= | ||
ENST00000361804.5:c.1412A= MANE Select | ENSP00000354720.5:p.Tyr471= | |
ENST00000361804.4:c.1412A= | ENSP00000354720.4:p.Tyr471= | |
NM_005445.3:c.1412A= , LRG_774t1:c.1412A= | NP_005436.1:p.Tyr471= | |
NM_005445.4:c.1412A= MANE Select | NP_005436.1:p.Tyr471= |