HGVS | Genome Assembly |
---|---|
NC_000007.14:g.93906158G>A , CM000669.2:g.93906158G>A | GRCh38 |
NC_000007.13:g.93535470G>A , CM000669.1:g.93535470G>A | GRCh37 |
NC_000007.12:g.93373406G>A | NCBI36 |
NG_051196.1:g.4651G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000455502.5:c.-11-578G>A | ENSP00000395857.1:n.-11-578G>A |