HGVS | Genome Assembly |
---|---|
NC_000014.9:g.75135041A>G , CM000676.2:g.75135041A>G | GRCh38 |
NC_000014.8:g.75601744A>G , CM000676.1:g.75601744A>G | GRCh37 |
NC_000014.7:g.74671497A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000303575.9:c.539-35T>C MANE Select | ENSP00000303145.4:n.539-35T>C | |
ENST00000303575.8:c.539-35T>C | ENSP00000303145.4:n.539-35T>C | |
ENST00000555036.1:n.322-35T>C | ||
ENST00000555873.1:c.*175-35T>C | ENSP00000450726.1:n.*175-35T>C | |
ENST00000556969.5:n.246-35T>C | ||
ENST00000557670.5:n.267-35T>C | ||
NM_006827.5:c.539-35T>C | NP_006818.3:n.539-35T>C | |
NM_006827.6:c.539-35T>C MANE Select | NP_006818.3:n.539-35T>C |