HGVS | Genome Assembly |
---|---|
NC_000008.11:g.38144407A= , CM000670.2:g.38144407A= | GRCh38 |
NC_000008.10:g.38001925A= , CM000670.1:g.38001925A= | GRCh37 |
NC_000008.9:g.38121082A= | NCBI36 |
NG_011827.1:g.11676T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000276449.9:c.745-21T= MANE Select | ENSP00000276449.3:n.745-21T= | |
ENST00000276449.8:c.745-21T= | ENSP00000276449.3:n.745-21T= | |
ENST00000520114.1:n.2693T= | ||
ENST00000522050.1:c.587-21T= | ||
NM_000349.2:c.745-21T= | NP_000340.2:n.745-21T= | |
XM_006716392.1:c.651-21T= | XP_006716455.1:n.651-21T= | |
NM_000349.3:c.745-21T= MANE Select | NP_000340.2:n.745-21T= |