HGVS | Genome Assembly |
---|---|
NC_000004.12:g.174106417T>C , CM000666.2:g.174106417T>C | GRCh38 |
NC_000004.11:g.175027568T>C , CM000666.1:g.175027568T>C | GRCh37 |
NC_000004.10:g.175264143T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
NR_125896.1:n.276-8588A>G | ||
XR_939484.1:n.877+18778T>C | ||
XR_939485.1:n.877+18778T>C |