HGVS | Genome Assembly |
---|---|
NC_000012.12:g.55522957T>C , CM000674.2:g.55522957T>C | GRCh38 |
NC_000012.11:g.55916741T>C , CM000674.1:g.55916741T>C | GRCh37 |
NC_000012.10:g.54203008T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000419708.1:n.365T>C (OR6C64P) | ||
XM_011538339.1:c.-147-29799A>G (OR6C70) | XP_011536641.1:n.-147-29799A>G | |
XM_011538340.1:c.-147-29799A>G (OR6C70) | XP_011536642.1:n.-147-29799A>G | |
XM_011538341.1:c.-147-29799A>G (OR6C70) | XP_011536643.1:n.-147-29799A>G |