HGVS | Genome Assembly |
---|---|
NC_000007.14:g.107683423T= , CM000669.2:g.107683423T= | GRCh38 |
NC_000007.13:g.107323868T= , CM000669.1:g.107323868T= | GRCh37 |
NC_000007.12:g.107111104T= | NCBI36 |
NG_008489.1:g.27789T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000644269.2:c.919-32T= MANE Select | ENSP00000494017.1:n.919-32T= | |
ENST00000265715.7:c.919-32T= | ENSP00000265715.3:n.919-32T= | |
NM_000441.1:c.919-32T= | NP_000432.1:n.919-32T= | |
XM_005250425.1:c.919-32T= | XP_005250482.1:n.919-32T= | |
XM_006716025.2:c.919-32T= | XP_006716088.1:n.919-32T= | |
XM_005250425.2:c.919-32T= | XP_005250482.1:n.919-32T= | |
XM_006716025.3:c.919-32T= | XP_006716088.1:n.919-32T= | |
XM_017012318.1:c.919-32T= | XP_016867807.1:n.919-32T= | |
NM_000441.2:c.919-32T= MANE Select | NP_000432.1:n.919-32T= |