HGVS | Genome Assembly |
---|---|
NC_000004.12:g.176666698T>C , CM000666.2:g.176666698T>C | GRCh38 |
NC_000004.11:g.177587849T>C , CM000666.1:g.177587849T>C | GRCh37 |
NC_000004.10:g.177824843T>C | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
XR_939498.1:n.121-2923T>C | ||
XR_939499.1:n.121-2923T>C | ||
XR_939498.2:n.208-2923T>C | ||
XR_939499.2:n.204-2923T>C |