HGVS | Genome Assembly |
---|---|
NC_000012.12:g.71269405C>T , CM000674.2:g.71269405C>T | GRCh38 |
NC_000012.11:g.71663185C>T , CM000674.1:g.71663185C>T | GRCh37 |
NC_000012.10:g.69949452C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000393330.6:c.-110+7946G>A | ENSP00000377003.2:n.-110+7946G>A | |
ENST00000549421.1:n.206+13311G>A |