HGVS | Genome Assembly |
---|---|
NC_000007.14:g.141973824T>C , CM000669.2:g.141973824T>C | GRCh38 |
NC_000007.13:g.141673624T>C , CM000669.1:g.141673624T>C | GRCh37 |
NC_000007.12:g.141320093T>C | NCBI36 |
NG_016141.1:g.4950A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000465654.5:c.-3+27827T>C (MGAM) | ENSP00000419372.1:n.-3+27827T>C | |
XM_011515783.1:c.*25-12572T>C (OR9A4) | XP_011514085.1:n.*25-12572T>C |