HGVS | Genome Assembly |
---|---|
NC_000006.12:g.9993469C= , CM000668.2:g.9993469C= | GRCh38 |
NC_000006.11:g.9993702C= , CM000668.1:g.9993702C= | GRCh37 |
NC_000006.10:g.10101688C= | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000472329.5:n.117-54120G= | ||
ENST00000481704.1:c.6-54120G= | ENSP00000418286.1:n.6-54120G= | |
ENST00000485268.1:c.-290-46007G= | ENSP00000417933.1:n.-290-46007G= | |
XM_011515036.1:c.123-54120G= | XP_011513338.1:n.123-54120G= | |
XM_017011612.1:c.6-54120G= | XP_016867101.1:n.6-54120G= | |
NR_170155.1:n.338-54120G= |