HGVS | Genome Assembly |
---|---|
NC_000004.12:g.42962902C= , CM000666.2:g.42962902C= | GRCh38 |
NC_000004.11:g.42964919C= , CM000666.1:g.42964919C= | GRCh37 |
NC_000004.10:g.42659676C= | NCBI36 |
NG_027718.1:g.74637C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000399770.3:c.395C= MANE Select | ENSP00000382670.2:p.Thr132= | |
ENST00000399770.2:c.395C= | ENSP00000382670.2:p.Thr132= | |
NM_001080476.2:c.395C= | NP_001073945.1:p.Thr132= | |
XM_011513691.1:c.32C= | XP_011511993.1:p.Thr11= | |
NM_001080476.3:c.395C= MANE Select | NP_001073945.1:p.Thr132= |