HGVS | Genome Assembly |
---|---|
NC_000001.11:g.196996092T= , CM000663.2:g.196996092T= | GRCh38 |
NC_000001.10:g.196965222T= , CM000663.1:g.196965222T= | GRCh37 |
NC_000001.9:g.195231845T= | NCBI36 |
NG_016365.1:g.23556T= , LRG_227:g.23556T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000699466.1:c.606T= | ENSP00000514393.1:p.Tyr202= | |
ENST00000699467.1:n.930T= | ||
ENST00000699468.1:c.-24-22T= | ENSP00000514394.1:n.-24-22T= | |
ENST00000256785.5:c.861T= MANE Select | ENSP00000256785.4:p.Tyr287= | |
ENST00000256785.4:c.861T= | ENSP00000256785.4:p.Tyr287= | |
NM_030787.3:c.861T= , LRG_227t1:c.861T= | NP_110414.1:p.Tyr287= | |
XM_011510020.1:c.870T= | XP_011508322.1:p.Tyr290= | |
XM_011510020.2:c.870T= | XP_011508322.1:p.Tyr290= | |
NM_030787.4:c.861T= MANE Select | NP_110414.1:p.Tyr287= |