HGVS | Genome Assembly |
---|---|
NC_000004.12:g.10035034T= , CM000666.2:g.10035034T= | GRCh38 |
NC_000004.11:g.10036658T= , CM000666.1:g.10036658T= | GRCh37 |
NC_000004.10:g.9645756T= | NCBI36 |
NG_011540.1:g.10215A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000309065.7:c.-41+5096A= | ENSP00000311383.3:n.-41+5096A= | |
ENST00000481042.1:n.1366A= | ||
ENST00000505104.5:n.81+5096A= | ||
ENST00000506583.5:c.-41+5096A= | ENSP00000422209.1:n.-41+5096A= | |
ENST00000513129.1:c.-40-9028A= | ENSP00000426800.1:n.-40-9028A= | |
NM_001001290.1:c.-41+5096A= | NP_001001290.1:n.-41+5096A= | |
XM_006713969.2:c.-41+5096A= | XP_006714032.1:n.-41+5096A= | |
XM_011513857.1:c.-41+5096A= | XP_011512159.1:n.-41+5096A= | |
NM_001001290.2:c.-41+5096A= | NP_001001290.1:n.-41+5096A= |