HGVS | Genome Assembly |
---|---|
NC_000020.11:g.57562882G= , CM000682.2:g.57562882G= | GRCh38 |
NC_000020.10:g.56137938G= , CM000682.1:g.56137938G= | GRCh37 |
NC_000020.9:g.55571344G= | NCBI36 |
NG_008205.1:g.6802G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000319441.6:c.593G= MANE Select | ENSP00000319814.4:p.Cys198= | |
ENST00000319441.5:c.593G= | ENSP00000319814.4:p.Cys198= | |
ENST00000467047.1:n.1803G= | ||
ENST00000470051.1:n.49G= | ||
ENST00000498194.1:n.535G= | ||
NM_002591.3:c.593G= | NP_002582.3:p.Cys198= | |
XM_011528839.1:c.197G= | XP_011527141.1:p.Cys66= | |
XM_024451888.1:c.197G= | XP_024307656.1:p.Cys66= | |
NM_002591.4:c.593G= MANE Select | NP_002582.3:p.Cys198= |