HGVS | Genome Assembly |
---|---|
NC_000023.11:g.136659219C= , CM000685.2:g.136659219C= | GRCh38 |
NC_000023.10:g.135741378C= , CM000685.1:g.135741378C= | GRCh37 |
NC_000023.9:g.135569044C= | NCBI36 |
NG_007280.1:g.16043C= , LRG_141:g.16043C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695724.1:c.*208C= | ENSP00000512122.1:n.*208C= | |
ENST00000695725.1:c.*145C= | ENSP00000512123.1:n.*145C= | |
ENST00000695726.1:n.2558C= | ||
ENST00000695729.1:n.3393C= | ||
ENST00000370629.7:c.590C= MANE Select | ENSP00000359663.2:p.Ser197= | |
ENST00000370628.2:c.527C= | ENSP00000359662.2:p.Ser176= | |
ENST00000370629.6:c.590C= | ENSP00000359663.2:p.Ser197= | |
NM_000074.2:c.590C= , LRG_141t1:c.590C= | NP_000065.1:p.Ser197= | |
NM_000074.3:c.590C= MANE Select | NP_000065.1:p.Ser197= |