HGVS | Genome Assembly |
---|---|
NC_000023.11:g.136659170C= , CM000685.2:g.136659170C= | GRCh38 |
NC_000023.10:g.135741329C= , CM000685.1:g.135741329C= | GRCh37 |
NC_000023.9:g.135568995C= | NCBI36 |
NG_007280.1:g.15994C= , LRG_141:g.15994C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695724.1:c.*159C= | ENSP00000512122.1:n.*159C= | |
ENST00000695725.1:c.*96C= | ENSP00000512123.1:n.*96C= | |
ENST00000695726.1:n.2509C= | ||
ENST00000695729.1:n.3344C= | ||
ENST00000370629.7:c.541C= MANE Select | ENSP00000359663.2:p.Arg181= | |
ENST00000370628.2:c.478C= | ENSP00000359662.2:p.Arg160= | |
ENST00000370629.6:c.541C= | ENSP00000359663.2:p.Arg181= | |
NM_000074.2:c.541C= , LRG_141t1:c.541C= | NP_000065.1:p.Arg181= | |
NM_000074.3:c.541C= MANE Select | NP_000065.1:p.Arg181= |