HGVS | Genome Assembly |
---|---|
NC_000003.12:g.74578567A>T , CM000665.2:g.74578567A>T | GRCh38 |
NC_000003.11:g.74627718A>T , CM000665.1:g.74627718A>T | GRCh37 |
NC_000003.10:g.74710408A>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263665.7:c.-81+35824T>A MANE Select | ENSP00000263665.6:n.-81+35824T>A | |
XM_005264757.2:c.-81+35824T>A | XP_005264814.1:n.-81+35824T>A | |
XM_005264758.2:c.-81+35824T>A | XP_005264815.1:n.-81+35824T>A | |
XM_005264757.3:c.-81+35824T>A | XP_005264814.1:n.-81+35824T>A | |
XM_017006507.1:c.-81+35181T>A | XP_016861996.1:n.-81+35181T>A | |
NM_001393376.1:c.-81+35181T>A | NP_001380305.1:n.-81+35181T>A | |
NM_020872.3:c.-81+35824T>A MANE Select | NP_065923.1:n.-81+35824T>A |