HGVS | Genome Assembly |
---|---|
NC_000011.10:g.65868552A>G , CM000673.2:g.65868552A>G | GRCh38 |
NC_000011.9:g.65636023A>G , CM000673.1:g.65636023A>G | GRCh37 |
NC_000011.8:g.65392599A>G | NCBI36 |
NG_012304.2:g.9383T>C | |
NG_053116.1:g.13491A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307998.11:c.805T>C MANE Select | ENSP00000309953.6:p.Cys269Arg | |
ENST00000307998.10:c.805T>C | ENSP00000309953.6:p.Cys269Arg | |
ENST00000526628.5:n.1371T>C | ||
ENST00000527969.1:n.1490T>C | ||
ENST00000528176.5:c.805T>C | ENSP00000434151.1:p.Cys269Arg | |
ENST00000531005.5:n.1799T>C | ||
ENST00000531972.5:c.805T>C | ENSP00000435295.1:p.Cys269Arg | |
ENST00000532084.5:n.231T>C | ||
NM_016938.4:c.805T>C | NP_058634.4:p.Cys269Arg | |
NR_037718.1:n.1064T>C | ||
NM_016938.5:c.805T>C MANE Select | NP_058634.4:p.Cys269Arg | |
NR_037718.2:n.930T>C |