HGVS | Genome Assembly |
---|---|
NC_000015.10:g.38252972G= , CM000677.2:g.38252972G= | GRCh38 |
NC_000015.9:g.38545173G= , CM000677.1:g.38545173G= | GRCh37 |
NC_000015.8:g.36332465G= | NCBI36 |
NG_008980.1:g.5122G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000299084.9:c.-214G= MANE Select | ENSP00000299084.4:n.-214G= | |
ENST00000299084.8:c.-214G= | ENSP00000299084.4:n.-214G= | |
ENST00000561205.1:n.125G= | ||
NM_152594.2:c.-214G= | NP_689807.1:n.-214G= | |
XM_005254202.2:c.-214G= | XP_005254259.1:n.-214G= | |
XM_005254203.3:c.-261G= | XP_005254260.1:n.-261G= | |
XM_005254202.3:c.-214G= | XP_005254259.1:n.-214G= | |
XR_001751484.1:n.87+595C= | ||
NM_152594.3:c.-214G= MANE Select | NP_689807.1:n.-214G= |