HGVS | Genome Assembly |
---|---|
NC_000004.12:g.99149642C>G , CM000666.2:g.99149642C>G | GRCh38 |
NC_000004.11:g.100070799C>G , CM000666.1:g.100070799C>G | GRCh37 |
NC_000004.10:g.100289822C>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000504581.1:n.170-6862G>C | ||
NR_037884.1:n.680-4903C>G |