HGVS | Genome Assembly |
---|---|
NC_000011.10:g.96258988C= , CM000673.2:g.96258988C= | GRCh38 |
NC_000011.9:g.95992152C= , CM000673.1:g.95992152C= | GRCh37 |
NC_000011.8:g.95631800C= | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000524717.6:c.513+82395G= MANE Select | ENSP00000434552.1:n.513+82395G= | |
ENST00000524717.5:c.513+82395G= | ENSP00000434552.1:n.513+82395G= | |
NM_032427.3:c.513+82395G= | NP_115803.1:n.513+82395G= | |
XM_011543024.1:c.-172+83920G= | XP_011541326.1:n.-172+83920G= | |
XM_011543025.1:c.513+82395G= | XP_011541327.1:n.513+82395G= | |
XM_011543024.3:c.-172+83920G= | XP_011541326.1:n.-172+83920G= | |
XM_011543025.2:c.513+82395G= | XP_011541327.1:n.513+82395G= | |
NM_032427.4:c.513+82395G= MANE Select | NP_115803.1:n.513+82395G= |