HGVS | Genome Assembly |
---|---|
NC_000012.12:g.64609189T>G , CM000674.2:g.64609189T>G | GRCh38 |
NC_000012.11:g.65002969T>G , CM000674.1:g.65002969T>G | GRCh37 |
NC_000012.10:g.63289236T>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000637125.1:c.294+67484T>G (RASSF3) | ENSP00000490100.1:n.294+67484T>G | |
XR_945027.1:n.1024+156A>C (RASSF3-DT) | ||
XR_945027.2:n.1045+156A>C (RASSF3-DT) |