HGVS | Genome Assembly |
---|---|
NC_000002.12:g.41534699A>C , CM000664.2:g.41534699A>C | GRCh38 |
NC_000002.11:g.41761839A>C , CM000664.1:g.41761839A>C | GRCh37 |
NC_000002.10:g.41615343A>C | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
XR_939996.1:n.181+3027T>G | ||
XR_939997.1:n.146+3027T>G | ||
XR_939997.2:n.9529+3027T>G |