HGVS | Genome Assembly |
---|---|
NC_000007.14:g.7968153T>C , CM000669.2:g.7968153T>C | GRCh38 |
NC_000007.13:g.8007784T>C , CM000669.1:g.8007784T>C | GRCh37 |
NC_000007.12:g.7974309T>C | NCBI36 |
NG_032073.1:g.4411T>C |
HGVS | Amino-acid Change | |
---|---|---|
NR_110018.1:n.209+391A>G |