HGVS | Genome Assembly |
---|---|
NC_000002.12:g.29071074C= , CM000664.2:g.29071074C= | GRCh38 |
NC_000002.11:g.29293940C= , CM000664.1:g.29293940C= | GRCh37 |
NC_000002.10:g.29147444C= | NCBI36 |
NG_021427.1:g.8188G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000331664.6:c.3188G= MANE Select | ENSP00000332809.4:p.Ser1063= | |
ENST00000331664.5:c.3188G= | ENSP00000332809.4:p.Ser1063= | |
NM_001029883.2:c.3188G= | NP_001025054.1:p.Ser1063= | |
XM_011532826.1:c.3188G= | XP_011531128.1:p.Ser1063= | |
XR_939901.1:n.185+1907C= | ||
XR_939902.1:n.173+1919C= | ||
NM_001029883.3:c.3188G= MANE Select | NP_001025054.1:p.Ser1063= |