HGVS | Genome Assembly |
---|---|
NC_000010.11:g.87863540G= , CM000672.2:g.87863540G= | GRCh38 |
NC_000010.10:g.89623297G= , CM000672.1:g.89623297G= | GRCh37 |
NC_000010.9:g.89613277G= | NCBI36 |
NG_007466.2:g.5103G= , LRG_311:g.5103G= | |
NG_033079.1:g.4898C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000706954.1:c.-17+898G= | ENSP00000516674.1:n.-17+898G= | |
ENST00000688308.1:c.-17+427G= | ENSP00000508752.1:n.-17+427G= | |
ENST00000693560.1:c.-410G= | ENSP00000509861.1:n.-410G= | |
ENST00000371953.7:c.-930G= | ENSP00000361021.3:n.-930G= | |
ENST00000610634.1:c.-1032G= | ENSP00000477517.1:n.-1032G= | |
NM_000314.5:c.-929G= | NP_000305.3:n.-929G= | |
NM_000314.6:c.-929G= | NP_000305.3:n.-929G= | |
NM_001304717.2:c.-410G= | NP_001291646.2:n.-410G= | |
NM_001304718.1:c.-1634G= | NP_001291647.1:n.-1634G= |