HGVS | Genome Assembly |
---|---|
NC_000011.10:g.89285145T= , CM000673.2:g.89285145T= | GRCh38 |
NC_000011.9:g.89018313T= , CM000673.1:g.89018313T= | GRCh37 |
NC_000011.8:g.88657961T= | NCBI36 |
NG_008748.1:g.112274T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263321.6:c.1366+191T= MANE Select | ENSP00000263321.4:n.1366+191T= | |
ENST00000263321.5:c.1366+191T= | ENSP00000263321.4:n.1366+191T= | |
ENST00000528243.1:n.364+191T= | ||
NM_000372.4:c.1366+191T= | NP_000363.1:n.1366+191T= | |
XM_011542970.1:c.1366+191T= | XP_011541272.1:n.1366+191T= | |
XM_011542970.2:c.1366+191T= | XP_011541272.1:n.1366+191T= | |
XR_001748321.1:n.2456+889A= | ||
XR_001748322.1:n.2457+889A= | ||
NM_000372.5:c.1366+191T= MANE Select | NP_000363.1:n.1366+191T= |