HGVS | Genome Assembly |
---|---|
NC_000008.11:g.38145126A= , CM000670.2:g.38145126A= | GRCh38 |
NC_000008.10:g.38002644A= , CM000670.1:g.38002644A= | GRCh37 |
NC_000008.9:g.38121801A= | NCBI36 |
NG_011827.1:g.10957T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000276449.9:c.744+96T= MANE Select | ENSP00000276449.3:n.744+96T= | |
ENST00000276449.8:c.744+96T= | ENSP00000276449.3:n.744+96T= | |
ENST00000520114.1:n.1974T= | ||
ENST00000522050.1:c.587-740T= | ||
NM_000349.2:c.744+96T= | NP_000340.2:n.744+96T= | |
XM_006716392.1:c.651-740T= | XP_006716455.1:n.651-740T= | |
NM_000349.3:c.744+96T= MANE Select | NP_000340.2:n.744+96T= |