HGVS | Genome Assembly |
---|---|
NC_000013.11:g.105464999T>C , CM000675.2:g.105464999T>C | GRCh38 |
NC_000013.10:g.106117348T>C , CM000675.1:g.106117348T>C | GRCh37 |
NC_000013.9:g.104915349T>C | NCBI36 |
NG_012694.1:g.4133T>C |
HGVS | Amino-acid Change | |
---|---|---|
NR_040247.1:n.739+1188A>G |