HGVS | Genome Assembly |
---|---|
NC_000008.11:g.86643612C= , CM000670.2:g.86643612C= | GRCh38 |
NC_000008.10:g.87655840C= , CM000670.1:g.87655840C= | GRCh37 |
NC_000008.9:g.87724956C= | NCBI36 |
NG_016980.1:g.105064G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000320005.6:c.1178+139G= MANE Select | ENSP00000316605.5:n.1178+139G= | |
ENST00000681546.1:n.998+139G= | ||
ENST00000681746.1:c.1178+139G= | ENSP00000505959.1:n.1178+139G= | |
ENST00000320005.5:c.1178+139G= | ENSP00000316605.5:n.1178+139G= | |
NM_019098.4:c.1178+139G= | NP_061971.3:n.1178+139G= | |
XM_011517138.1:c.764+139G= | XP_011515440.1:n.764+139G= | |
XM_011517138.2:c.764+139G= | XP_011515440.1:n.764+139G= | |
NM_019098.5:c.1178+139G= MANE Select | NP_061971.3:n.1178+139G= |