HGVS | Genome Assembly |
---|---|
NC_000013.11:g.27924663T>A , CM000675.2:g.27924663T>A | GRCh38 |
NC_000013.10:g.28498800T>A , CM000675.1:g.28498800T>A | GRCh37 |
NC_000013.9:g.27396800T>A | NCBI36 |
NG_008183.1:g.9633T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000381033.5:c.814T>A MANE Select | ENSP00000370421.4:p.Ser272Thr | |
ENST00000381033.4:c.814T>A | ENSP00000370421.4:p.Ser272Thr | |
NM_000209.3:c.814T>A | NP_000200.1:p.Ser272Thr | |
NM_000209.4:c.814T>A MANE Select | NP_000200.1:p.Ser272Thr |