HGVS | Genome Assembly |
---|---|
NC_000016.10:g.172849T>C , CM000678.2:g.172849T>C | GRCh38 |
NC_000016.9:g.222848T>C , CM000678.1:g.222848T>C | GRCh37 |
NC_000016.8:g.162848T>C | NCBI36 |
NG_000006.1:g.33712T>C | |
NG_059186.1:g.1199T>C | |
NG_059271.1:g.5003T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000251595.10:c.-64T>C | ENSP00000251595.6:n.-64T>C | |
NM_000517.4:c.-64T>C | NP_000508.1:n.-64T>C |