HGVS | Genome Assembly |
---|---|
NC_000010.11:g.110812779A>T , CM000672.2:g.110812779A>T | GRCh38 |
NC_000010.10:g.112572537A>T , CM000672.1:g.112572537A>T | GRCh37 |
NC_000010.9:g.112562527A>T | NCBI36 |
NG_021177.1:g.173383A>T , LRG_382:g.173383A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000369519.4:c.2382A>T MANE Select | ENSP00000358532.3:p.Arg794Ser | |
ENST00000369519.3:c.2382A>T | ENSP00000358532.3:p.Arg794Ser | |
NM_001134363.2:c.2382A>T | NP_001127835.2:p.Arg794Ser | |
XM_011539697.1:c.1998A>T | XP_011537999.1:p.Arg666Ser | |
XM_017016103.2:c.2217A>T | XP_016871592.1:p.Arg739Ser | |
XM_017016104.2:c.1998A>T | XP_016871593.1:p.Arg666Ser | |
NM_001134363.3:c.2382A>T MANE Select | NP_001127835.2:p.Arg794Ser |