HGVS | Genome Assembly |
---|---|
NC_000014.9:g.102129288A>T , CM000676.2:g.102129288A>T | GRCh38 |
NC_000014.8:g.102595625A>T , CM000676.1:g.102595625A>T | GRCh37 |
NC_000014.7:g.101665378A>T | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000334701.11:c.155+9962T>A | ENSP00000335153.7:n.155+9962T>A | |
ENST00000557234.1:c.155+9962T>A | ENSP00000452241.1:n.155+9962T>A | |
ENST00000558600.1:c.155+9962T>A | ENSP00000489370.1:n.155+9962T>A | |
NM_001017963.2:c.155+9962T>A | NP_001017963.2:n.155+9962T>A | |
XM_011536718.1:c.155+9962T>A | XP_011535020.1:n.155+9962T>A | |
XM_011536718.2:c.155+9962T>A | XP_011535020.1:n.155+9962T>A | |
NM_001017963.3:c.155+9962T>A | NP_001017963.2:n.155+9962T>A |