HGVS | Genome Assembly |
---|---|
NC_000012.12:g.10446003A>C , CM000674.2:g.10446003A>C | GRCh38 |
NC_000012.11:g.10598602A>C , CM000674.1:g.10598602A>C | GRCh37 |
NC_000012.10:g.10489869A>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000536188.5:c.685+565T>G | ENSP00000441432.1:n.685+565T>G | |
NM_001304448.1:c.685+565T>G | NP_001291377.1:n.685+565T>G | |
XM_024448973.1:c.685+565T>G | XP_024304741.1:n.685+565T>G |