HGVS | Genome Assembly |
---|---|
NC_000010.11:g.63577278C>G , CM000672.2:g.63577278C>G | GRCh38 |
NC_000010.10:g.65337038C>G , CM000672.1:g.65337038C>G | GRCh37 |
NC_000010.9:g.65007044C>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000373758.5:c.105+10868C>G MANE Select | ENSP00000362863.4:n.105+10868C>G | |
ENST00000373758.4:c.105+10868C>G | ENSP00000362863.4:n.105+10868C>G | |
NM_001001330.2:c.105+10868C>G | NP_001001330.1:n.105+10868C>G | |
XM_011539501.1:c.105+10868C>G | XP_011537803.1:n.105+10868C>G | |
XM_011539501.2:c.105+10868C>G | XP_011537803.1:n.105+10868C>G | |
XM_017015896.1:c.105+10868C>G | XP_016871385.1:n.105+10868C>G | |
NM_001001330.3:c.105+10868C>G MANE Select | NP_001001330.1:n.105+10868C>G |