HGVS | Genome Assembly |
---|---|
NC_000015.10:g.78818751C>T , CM000677.2:g.78818751C>T | GRCh38 |
NC_000015.9:g.79111093C>T , CM000677.1:g.79111093C>T | GRCh37 |
NC_000015.8:g.76898148C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000379535.8:c.-10+7710C>T | ENSP00000368850.4:n.-10+7710C>T |