HGVS | Genome Assembly |
---|---|
NC_000012.12:g.55523086A>T , CM000674.2:g.55523086A>T | GRCh38 |
NC_000012.11:g.55916870A>T , CM000674.1:g.55916870A>T | GRCh37 |
NC_000012.10:g.54203137A>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000419708.1:n.494A>T (OR6C64P) | ||
XM_011538339.1:c.-147-29928T>A (OR6C70) | XP_011536641.1:n.-147-29928T>A | |
XM_011538340.1:c.-147-29928T>A (OR6C70) | XP_011536642.1:n.-147-29928T>A | |
XM_011538341.1:c.-147-29928T>A (OR6C70) | XP_011536643.1:n.-147-29928T>A |