HGVS | Genome Assembly |
---|---|
NC_000008.11:g.96145197G>A , CM000670.2:g.96145197G>A | GRCh38 |
NC_000008.10:g.97157425G>A , CM000670.1:g.97157425G>A | GRCh37 |
NC_000008.9:g.97226601G>A | NCBI36 |
NG_008981.1:g.20596C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000287020.7:c.734C>T MANE Select | ENSP00000287020.4:p.Ala245Val | |
ENST00000287020.6:c.734C>T | ENSP00000287020.4:p.Ala245Val | |
ENST00000620978.1:c.706+28C>T | ENSP00000480170.1:n.706+28C>T | |
ENST00000621429.1:c.734C>T | ENSP00000483711.1:p.Ala245Val | |
NM_001001557.2:c.734C>T | NP_001001557.1:p.Ala245Val | |
XM_011517030.1:c.335C>T | XP_011515332.1:p.Ala112Val | |
NM_001001557.3:c.734C>T | NP_001001557.1:p.Ala245Val | |
NM_001001557.4:c.734C>T MANE Select | NP_001001557.1:p.Ala245Val |