HGVS | Genome Assembly |
---|---|
NC_000022.11:g.20242465C>A , CM000684.2:g.20242465C>A | GRCh38 |
NC_000022.10:g.20229988C>A , CM000684.1:g.20229988C>A | GRCh37 |
NC_000022.9:g.18609988C>A | NCBI36 |
NG_012176.1:g.30829G>T | |
NG_012176.2:g.30829G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000043402.8:c.668G>T MANE Select | ENSP00000043402.7:p.Arg223Leu | |
ENST00000043402.7:c.668G>T | ENSP00000043402.7:p.Arg223Leu | |
ENST00000416372.5:c.727G>T | ||
ENST00000425986.1:c.925G>T | ||
NM_023004.5:c.668G>T | NP_075380.1:p.Arg223Leu | |
NM_023004.6:c.668G>T MANE Select | NP_075380.1:p.Arg223Leu |