HGVS | Genome Assembly |
---|---|
NC_000007.14:g.141973894T>A , CM000669.2:g.141973894T>A | GRCh38 |
NC_000007.13:g.141673694T>A , CM000669.1:g.141673694T>A | GRCh37 |
NC_000007.12:g.141320163T>A | NCBI36 |
NG_016141.1:g.4880A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000465654.5:c.-3+27897T>A (MGAM) | ENSP00000419372.1:n.-3+27897T>A | |
XM_011515783.1:c.*25-12502T>A (OR9A4) | XP_011514085.1:n.*25-12502T>A |