HGVS | Genome Assembly |
---|---|
NC_000017.11:g.40100440G= , CM000679.2:g.40100440G= | GRCh38 |
NC_000017.10:g.38256693G= , CM000679.1:g.38256693G= | GRCh37 |
NC_000017.9:g.35510219G= | NCBI36 |
NG_033084.1:g.5286C= |
HGVS | Amino-acid Change |
---|---|
NM_021724.5:c.-346C= MANE Select | NP_068370.1:n.-346C= |
ENST00000246672.4:c.-346C= MANE Select | ENSP00000246672.3:n.-346C= |
NM_021724.4:c.-346C= | NP_068370.1:n.-346C= |
ENST00000246672.3:c.-346C= | ENSP00000246672.3:n.-346C= |