HGVS | Genome Assembly |
---|---|
NC_000002.12:g.118079775T>C , CM000664.2:g.118079775T>C | GRCh38 |
NC_000002.11:g.118837351T>C , CM000664.1:g.118837351T>C | GRCh37 |
NC_000002.10:g.118553821T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
XM_011512305.1:c.697-2243A>G | XP_011510607.1:n.697-2243A>G | |
XR_001739662.2:n.138+8476A>G |