HGVS | Genome Assembly |
---|---|
NC_000004.12:g.10034652del , CM000666.2:g.10034652del | GRCh38 |
NC_000004.11:g.10036276del , CM000666.1:g.10036276del | GRCh37 |
NC_000004.10:g.9645374del | NCBI36 |
NG_011540.1:g.10597del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000309065.7:c.-41+5478del | ENSP00000311383.3:n.-41+5478del | |
ENST00000481042.1:n.1748del | ||
ENST00000505104.5:n.81+5478del | ||
ENST00000506583.5:c.-41+5478del | ENSP00000422209.1:n.-41+5478del | |
ENST00000513129.1:c.-40-8646del | ENSP00000426800.1:n.-40-8646del | |
NM_001001290.1:c.-41+5478del | NP_001001290.1:n.-41+5478del | |
XM_006713969.2:c.-41+5478del | XP_006714032.1:n.-41+5478del | |
XM_011513857.1:c.-41+5478del | XP_011512159.1:n.-41+5478del | |
NM_001001290.2:c.-41+5478del | NP_001001290.1:n.-41+5478del |