HGVS | Genome Assembly |
---|---|
NC_000022.11:g.23573091T>C , CM000684.2:g.23573091T>C | GRCh38 |
NC_000022.10:g.23915278T>C , CM000684.1:g.23915278T>C | GRCh37 |
NC_000022.9:g.22245278T>C | NCBI36 |
NG_009791.1:g.12218A>G , LRG_69:g.12218A>G |
HGVS | Amino-acid Change | |
---|---|---|
XR_938078.1:n.696T>C | ||
XR_938078.2:n.1280T>C |