HGVS | Genome Assembly |
---|---|
NC_000004.12:g.177442669T>C , CM000666.2:g.177442669T>C | GRCh38 |
NC_000004.11:g.178363823T>C , CM000666.1:g.178363823T>C | GRCh37 |
NC_000004.10:g.178600817T>C | NCBI36 |
NG_011845.2:g.4835A>G |
HGVS | Amino-acid Change | |
---|---|---|
XR_001741929.1:n.82+88T>C |