HGVS | Genome Assembly |
---|---|
NC_000007.14:g.107689048A= , CM000669.2:g.107689048A= | GRCh38 |
NC_000007.13:g.107329493A= , CM000669.1:g.107329493A= | GRCh37 |
NC_000007.12:g.107116729A= | NCBI36 |
NG_008489.1:g.33414A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000644269.2:c.1002-5A= MANE Select | ENSP00000494017.1:n.1002-5A= | |
ENST00000265715.7:c.1002-5A= | ENSP00000265715.3:n.1002-5A= | |
NM_000441.1:c.1002-5A= | NP_000432.1:n.1002-5A= | |
XM_005250425.1:c.1002-5A= | XP_005250482.1:n.1002-5A= | |
XM_006716025.2:c.1002-5A= | XP_006716088.1:n.1002-5A= | |
XM_005250425.2:c.1002-5A= | XP_005250482.1:n.1002-5A= | |
XM_006716025.3:c.1002-5A= | XP_006716088.1:n.1002-5A= | |
XM_017012318.1:c.1002-5A= | XP_016867807.1:n.1002-5A= | |
NM_000441.2:c.1002-5A= MANE Select | NP_000432.1:n.1002-5A= |