HGVS | Genome Assembly |
---|---|
NC_000012.12:g.7690177G>A , CM000674.2:g.7690177G>A | GRCh38 |
NC_000012.11:g.7842773G>A , CM000674.1:g.7842773G>A | GRCh37 |
NC_000012.10:g.7734040G>A | NCBI36 |
NG_028167.1:g.10588C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000329913.4:c.796C>T MANE Select | ENSP00000331745.3:p.Arg266Cys | |
ENST00000329913.3:c.796C>T | ENSP00000331745.3:p.Arg266Cys | |
NM_020634.1:c.796C>T | NP_065685.1:p.Arg266Cys | |
NM_020634.2:c.796C>T | NP_065685.1:p.Arg266Cys | |
NM_020634.3:c.796C>T MANE Select | NP_065685.1:p.Arg266Cys |