HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154997038T>A , CM000685.2:g.154997038T>A | GRCh38 |
NC_000023.10:g.154225313T>A , CM000685.1:g.154225313T>A | GRCh37 |
NC_000023.9:g.153878507T>A | NCBI36 |
NG_011403.1:g.30686A>T | |
NG_011403.2:g.30686A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360256.9:c.323A>T MANE Select | ENSP00000353393.4:p.Lys108Met | |
ENST00000647125.1:c.*109A>T | ENSP00000496062.1:n.*109A>T | |
ENST00000360256.8:c.323A>T | ENSP00000353393.4:p.Lys108Met | |
ENST00000423959.5:c.218A>T | ENSP00000409446.1:p.Lys73Met | |
ENST00000453950.1:c.305A>T | ENSP00000389153.1:p.Lys102Met | |
NM_000132.3:c.323A>T | NP_000123.1:p.Lys108Met | |
XM_011531126.1:c.218A>T | XP_011529428.1:p.Lys73Met | |
NM_000132.4:c.323A>T MANE Select | NP_000123.1:p.Lys108Met |