HGVS | Genome Assembly |
---|---|
NC_000016.10:g.8797688A>G , CM000678.2:g.8797688A>G | GRCh38 |
NC_000016.9:g.8891545A>G , CM000678.1:g.8891545A>G | GRCh37 |
NC_000016.8:g.8799046A>G | NCBI36 |
NG_009209.1:g.4876A>G | |
NG_033146.1:g.4961T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000566983.5:c.-15-4111A>G | ENSP00000457956.1:n.-15-4111A>G |