HGVS | Genome Assembly |
---|---|
NC_000010.11:g.63577535C= , CM000672.2:g.63577535C= | GRCh38 |
NC_000010.10:g.65337295C= , CM000672.1:g.65337295C= | GRCh37 |
NC_000010.9:g.65007301C= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000373758.5:c.105+11125C= MANE Select | ENSP00000362863.4:n.105+11125C= | |
ENST00000373758.4:c.105+11125C= | ENSP00000362863.4:n.105+11125C= | |
NM_001001330.2:c.105+11125C= | NP_001001330.1:n.105+11125C= | |
XM_011539501.1:c.105+11125C= | XP_011537803.1:n.105+11125C= | |
XM_011539501.2:c.105+11125C= | XP_011537803.1:n.105+11125C= | |
XM_017015896.1:c.105+11125C= | XP_016871385.1:n.105+11125C= | |
NM_001001330.3:c.105+11125C= MANE Select | NP_001001330.1:n.105+11125C= |