HGVS | Genome Assembly |
---|---|
NC_000017.11:g.66239706T>A , CM000679.2:g.66239706T>A | GRCh38 |
NC_000017.10:g.64235824T>A , CM000679.1:g.64235824T>A | GRCh37 |
NC_000017.9:g.61666286T>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000577982.1:c.-43-10284A>T | ENSP00000464301.1:n.-43-10284A>T |