HGVS | Genome Assembly |
---|---|
NC_000023.11:g.74421964G>T , CM000685.2:g.74421964G>T | GRCh38 |
NC_000023.10:g.73641799G>T , CM000685.1:g.73641799G>T | GRCh37 |
NC_000023.9:g.73558524G>T | NCBI36 |
NG_011641.1:g.5715G>T | |
NG_011641.2:g.5715G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000587091.6:c.327G>T MANE Select | ENSP00000465734.1:p.Trp109Cys | |
ENST00000636771.1:c.73G>T | ||
ENST00000587091.5:c.327G>T | ENSP00000465734.1:p.Trp109Cys | |
NM_006517.4:c.327G>T | NP_006508.2:p.Trp109Cys | |
XM_005262294.1:c.327G>T | XP_005262351.1:p.Trp109Cys | |
XM_011531015.1:c.327G>T | XP_011529317.1:p.Trp109Cys | |
NM_006517.5:c.327G>T MANE Select | NP_006508.2:p.Trp109Cys |