HGVS | Genome Assembly |
---|---|
NC_000008.11:g.96144675C>A , CM000670.2:g.96144675C>A | GRCh38 |
NC_000008.10:g.97156903C>A , CM000670.1:g.97156903C>A | GRCh37 |
NC_000008.9:g.97226079C>A | NCBI36 |
NG_008981.1:g.21118G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000287020.7:c.1256G>T MANE Select | ENSP00000287020.4:p.Cys419Phe | |
ENST00000287020.6:c.1256G>T | ENSP00000287020.4:p.Cys419Phe | |
ENST00000620978.1:c.796G>T | ENSP00000480170.1:p.Ala266Ser | |
ENST00000621429.1:c.1005G>T | ENSP00000483711.1:p.Leu335= | |
NM_001001557.2:c.1256G>T | NP_001001557.1:p.Cys419Phe | |
XM_011517030.1:c.857G>T | XP_011515332.1:p.Cys286Phe | |
NM_001001557.3:c.1256G>T | NP_001001557.1:p.Cys419Phe | |
NM_001001557.4:c.1256G>T MANE Select | NP_001001557.1:p.Cys419Phe |