HGVS | Genome Assembly |
---|---|
NC_000003.12:g.74578614A>C , CM000665.2:g.74578614A>C | GRCh38 |
NC_000003.11:g.74627765A>C , CM000665.1:g.74627765A>C | GRCh37 |
NC_000003.10:g.74710455A>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263665.7:c.-81+35777T>G MANE Select | ENSP00000263665.6:n.-81+35777T>G | |
XM_005264757.2:c.-81+35777T>G | XP_005264814.1:n.-81+35777T>G | |
XM_005264758.2:c.-81+35777T>G | XP_005264815.1:n.-81+35777T>G | |
XM_005264757.3:c.-81+35777T>G | XP_005264814.1:n.-81+35777T>G | |
XM_017006507.1:c.-81+35134T>G | XP_016861996.1:n.-81+35134T>G | |
NM_001393376.1:c.-81+35134T>G | NP_001380305.1:n.-81+35134T>G | |
NM_020872.3:c.-81+35777T>G MANE Select | NP_065923.1:n.-81+35777T>G |