HGVS | Genome Assembly |
---|---|
NC_000011.10:g.89285100T= , CM000673.2:g.89285100T= | GRCh38 |
NC_000011.9:g.89018268T= , CM000673.1:g.89018268T= | GRCh37 |
NC_000011.8:g.88657916T= | NCBI36 |
NG_008748.1:g.112229T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263321.6:c.1366+146T= MANE Select | ENSP00000263321.4:n.1366+146T= | |
ENST00000263321.5:c.1366+146T= | ENSP00000263321.4:n.1366+146T= | |
ENST00000528243.1:n.364+146T= | ||
NM_000372.4:c.1366+146T= | NP_000363.1:n.1366+146T= | |
XM_011542970.1:c.1366+146T= | XP_011541272.1:n.1366+146T= | |
XM_011542970.2:c.1366+146T= | XP_011541272.1:n.1366+146T= | |
XR_001748321.1:n.2456+934A= | ||
XR_001748322.1:n.2457+934A= | ||
NM_000372.5:c.1366+146T= MANE Select | NP_000363.1:n.1366+146T= |