HGVS | Genome Assembly |
---|---|
NC_000008.11:g.104379328G>A , CM000670.2:g.104379328G>A | GRCh38 |
NC_000008.10:g.105391556G>A , CM000670.1:g.105391556G>A | GRCh37 |
NC_000008.9:g.105460732G>A | NCBI36 |
NG_008840.1:g.92722C>T | |
NG_008840.2:g.92722C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000521601.1:n.328+1856C>T |