HGVS | Genome Assembly |
---|---|
NC_000010.11:g.87863543A= , CM000672.2:g.87863543A= | GRCh38 |
NC_000010.10:g.89623300A= , CM000672.1:g.89623300A= | GRCh37 |
NC_000010.9:g.89613280A= | NCBI36 |
NG_007466.2:g.5106A= , LRG_311:g.5106A= | |
NG_033079.1:g.4895T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000706954.1:c.-17+901A= | ENSP00000516674.1:n.-17+901A= | |
ENST00000688308.1:c.-17+430A= | ENSP00000508752.1:n.-17+430A= | |
ENST00000693560.1:c.-407A= | ENSP00000509861.1:n.-407A= | |
ENST00000371953.7:c.-927A= | ENSP00000361021.3:n.-927A= | |
ENST00000610634.1:c.-1029A= | ENSP00000477517.1:n.-1029A= | |
NM_000314.5:c.-926A= | NP_000305.3:n.-926A= | |
NM_000314.6:c.-926A= | NP_000305.3:n.-926A= | |
NM_001304717.2:c.-407A= | NP_001291646.2:n.-407A= | |
NM_001304718.1:c.-1631A= | NP_001291647.1:n.-1631A= |