HGVS | Genome Assembly |
---|---|
NC_000007.14:g.141927246G>T , CM000669.2:g.141927246G>T | GRCh38 |
NC_000007.13:g.141627046G>T , CM000669.1:g.141627046G>T | GRCh37 |
NC_000007.12:g.141273515G>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000465654.5:c.-179-18575G>T (MGAM) | ENSP00000419372.1:n.-179-18575G>T | |
ENST00000497554.1:n.37-2531G>T (MGAM) | ||
XM_011515783.1:c.*24+7402G>T (OR9A4) | XP_011514085.1:n.*24+7402G>T |