HGVS | Genome Assembly |
---|---|
NC_000010.11:g.110780984C>T , CM000672.2:g.110780984C>T | GRCh38 |
NC_000010.10:g.112540742C>T , CM000672.1:g.112540742C>T | GRCh37 |
NC_000010.9:g.112530732C>T | NCBI36 |
NG_021177.1:g.141588C>T , LRG_382:g.141588C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369519.4:c.375C>T MANE Select | ENSP00000358532.3:p.Ser125= | |
ENST00000369519.3:c.375C>T | ENSP00000358532.3:p.Ser125= | |
NM_001134363.2:c.375C>T | NP_001127835.2:p.Ser125= | |
XM_011539697.1:c.-10C>T | XP_011537999.1:n.-10C>T | |
XM_017016103.2:c.210C>T | XP_016871592.1:p.Ser70= | |
XM_017016104.2:c.-10C>T | XP_016871593.1:n.-10C>T | |
NM_001134363.3:c.375C>T MANE Select | NP_001127835.2:p.Ser125= |