HGVS | Genome Assembly |
---|---|
NC_000023.11:g.136659415A= , CM000685.2:g.136659415A= | GRCh38 |
NC_000023.10:g.135741574A= , CM000685.1:g.135741574A= | GRCh37 |
NC_000023.9:g.135569240A= | NCBI36 |
NG_007280.1:g.16239A= , LRG_141:g.16239A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695724.1:c.*404A= | ENSP00000512122.1:n.*404A= | |
ENST00000695725.1:c.*341A= | ENSP00000512123.1:n.*341A= | |
ENST00000695726.1:n.2754A= | ||
ENST00000695729.1:n.3589A= | ||
ENST00000370629.7:c.786A= MANE Select | ENSP00000359663.2:p.Ter262= | |
ENST00000370628.2:c.723A= | ENSP00000359662.2:p.Ter241= | |
ENST00000370629.6:c.786A= | ENSP00000359663.2:p.Ter262= | |
NM_000074.2:c.786A= , LRG_141t1:c.786A= | NP_000065.1:p.Ter262= | |
NM_000074.3:c.786A= MANE Select | NP_000065.1:p.Ter262= |