HGVS | Genome Assembly |
---|---|
NC_000009.12:g.97069874C>A , CM000671.2:g.97069874C>A | GRCh38 |
NC_000009.11:g.99832156C>A , CM000671.1:g.99832156C>A | GRCh37 |
NC_000009.10:g.98871977C>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000679551.1:n.164-9903G>T | ||
ENST00000681517.1:n.315-9903G>T |