HGVS | Genome Assembly |
---|---|
NC_000009.12:g.120923941C= , CM000671.2:g.120923941C= | GRCh38 |
NC_000009.11:g.123686219C= , CM000671.1:g.123686219C= | GRCh37 |
NC_000009.10:g.122726040C= | NCBI36 |
NG_023346.1:g.10233G= |
HGVS | Amino-acid Change |
---|---|
NM_005658.5:c.141-149G= MANE Select | NP_005649.1:n.141-149G= |
ENST00000373887.8:c.141-149G= MANE Select | ENSP00000362994.3:n.141-149G= |
NM_001190945.1:c.141-149G= | NP_001177874.1:n.141-149G= |
NM_001190945.2:c.141-149G= | NP_001177874.1:n.141-149G= |
NM_005658.4:c.141-149G= | NP_005649.1:n.141-149G= |
ENST00000373887.7:c.141-149G= | ENSP00000362994.3:n.141-149G= |
ENST00000540010.1:c.141-149G= | ENSP00000443183.1:n.141-149G= |