HGVS | Genome Assembly |
---|---|
NC_000007.14:g.141973861T>G , CM000669.2:g.141973861T>G | GRCh38 |
NC_000007.13:g.141673661T>G , CM000669.1:g.141673661T>G | GRCh37 |
NC_000007.12:g.141320130T>G | NCBI36 |
NG_016141.1:g.4913A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000465654.5:c.-3+27864T>G (MGAM) | ENSP00000419372.1:n.-3+27864T>G | |
XM_011515783.1:c.*25-12535T>G (OR9A4) | XP_011514085.1:n.*25-12535T>G |