HGVS | Genome Assembly |
---|---|
NC_000019.10:g.11077477A>T , CM000681.2:g.11077477A>T | GRCh38 |
NC_000019.9:g.11188153A>T , CM000681.1:g.11188153A>T | GRCh37 |
NC_000019.8:g.11049153A>T | NCBI36 |
NG_011556.3:g.121546A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000645236.1:c.1458-1520A>T |