HGVS | Genome Assembly |
---|---|
NC_000012.12:g.55522925T>A , CM000674.2:g.55522925T>A | GRCh38 |
NC_000012.11:g.55916709T>A , CM000674.1:g.55916709T>A | GRCh37 |
NC_000012.10:g.54202976T>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000419708.1:n.333T>A (OR6C64P) | ||
XM_011538339.1:c.-147-29767A>T (OR6C70) | XP_011536641.1:n.-147-29767A>T | |
XM_011538340.1:c.-147-29767A>T (OR6C70) | XP_011536642.1:n.-147-29767A>T | |
XM_011538341.1:c.-147-29767A>T (OR6C70) | XP_011536643.1:n.-147-29767A>T |