HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154992944C= , CM000685.2:g.154992944C= | GRCh38 |
NC_000023.10:g.154221219C= , CM000685.1:g.154221219C= | GRCh37 |
NC_000023.9:g.153874413C= | NCBI36 |
NG_011403.1:g.34780G= | |
NG_011403.2:g.34780G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360256.9:c.593G= MANE Select | ENSP00000353393.4:p.Cys198= | |
ENST00000647125.1:c.*379G= | ENSP00000496062.1:n.*379G= | |
ENST00000360256.8:c.593G= | ENSP00000353393.4:p.Cys198= | |
ENST00000423959.5:c.488G= | ENSP00000409446.1:p.Cys163= | |
NM_000132.3:c.593G= | NP_000123.1:p.Cys198= | |
XM_011531126.1:c.488G= | XP_011529428.1:p.Cys163= | |
NM_000132.4:c.593G= MANE Select | NP_000123.1:p.Cys198= |