HGVS | Genome Assembly |
---|---|
NC_000010.11:g.110812682A>C , CM000672.2:g.110812682A>C | GRCh38 |
NC_000010.10:g.112572440A>C , CM000672.1:g.112572440A>C | GRCh37 |
NC_000010.9:g.112562430A>C | NCBI36 |
NG_021177.1:g.173286A>C , LRG_382:g.173286A>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000369519.4:c.2285A>C MANE Select | ENSP00000358532.3:p.Lys762Thr | |
ENST00000369519.3:c.2285A>C | ENSP00000358532.3:p.Lys762Thr | |
NM_001134363.2:c.2285A>C | NP_001127835.2:p.Lys762Thr | |
XM_011539697.1:c.1901A>C | XP_011537999.1:p.Lys634Thr | |
XM_017016103.2:c.2120A>C | XP_016871592.1:p.Lys707Thr | |
XM_017016104.2:c.1901A>C | XP_016871593.1:p.Lys634Thr | |
NM_001134363.3:c.2285A>C MANE Select | NP_001127835.2:p.Lys762Thr |