HGVS | Genome Assembly |
---|---|
NC_000012.12:g.55523093T>C , CM000674.2:g.55523093T>C | GRCh38 |
NC_000012.11:g.55916877T>C , CM000674.1:g.55916877T>C | GRCh37 |
NC_000012.10:g.54203144T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000419708.1:n.501T>C (OR6C64P) | ||
XM_011538339.1:c.-147-29935A>G (OR6C70) | XP_011536641.1:n.-147-29935A>G | |
XM_011538340.1:c.-147-29935A>G (OR6C70) | XP_011536642.1:n.-147-29935A>G | |
XM_011538341.1:c.-147-29935A>G (OR6C70) | XP_011536643.1:n.-147-29935A>G |