HGVS | Genome Assembly |
---|---|
NC_000001.11:g.113812320T>G , CM000663.2:g.113812320T>G | GRCh38 |
NC_000001.10:g.114354942T>G , CM000663.1:g.114354942T>G | GRCh37 |
NC_000001.9:g.114156465T>G | NCBI36 |
NG_011432.1:g.64434A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261441.9:c.93A>C MANE Select | ENSP00000261441.5:p.Arg31= | |
ENST00000612242.4:c.93A>C | ENSP00000479490.1:p.Arg31= | |
NM_018364.4:c.93A>C | NP_060834.2:p.Arg31= | |
NR_130896.1:n.157A>C | ||
XM_017001518.2:c.93A>C | XP_016857007.1:p.Arg31= | |
NM_018364.5:c.93A>C MANE Select | NP_060834.2:p.Arg31= | |
NR_130896.2:n.157A>C |