HGVS | Genome Assembly |
---|---|
NC_000012.12:g.68202881T= , CM000674.2:g.68202881T= | GRCh38 |
NC_000012.11:g.68596661T= , CM000674.1:g.68596661T= | GRCh37 |
NC_000012.10:g.66882928T= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000229134.5:c.364-798A= MANE Select | ENSP00000229134.4:n.364-798A= | |
ENST00000229134.4:c.364-798A= | ENSP00000229134.4:n.364-798A= | |
NM_018402.1:c.364-798A= | NP_060872.1:n.364-798A= | |
XM_011538568.1:c.364-798A= | XP_011536870.1:n.364-798A= | |
XR_945055.1:n.264+4153T= | ||
XR_002957418.1:n.280+4153T= | ||
NM_018402.2:c.364-798A= MANE Select | NP_060872.1:n.364-798A= |