HGVS | Genome Assembly |
---|---|
NC_000010.11:g.97877748C= , CM000672.2:g.97877748C= | GRCh38 |
NC_000010.10:g.99637505C= , CM000672.1:g.99637505C= | GRCh37 |
NC_000010.9:g.99627495C= | NCBI36 |
NG_029831.1:g.158081G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370597.8:c.1819+2501G= MANE Select | ENSP00000359629.3:n.1819+2501G= | |
ENST00000370597.7:c.1819+2501G= | ENSP00000359629.3:n.1819+2501G= | |
ENST00000413387.5:c.1464+2501G= | ENSP00000408445.1:n.1464+2501G= | |
NM_018058.6:c.1819+2501G= | NP_060528.3:n.1819+2501G= | |
XM_011539917.1:c.1819+2501G= | XP_011538219.1:n.1819+2501G= | |
XM_017016366.1:c.1819+2501G= | XP_016871855.1:n.1819+2501G= | |
XM_017016367.1:c.1819+2501G= | XP_016871856.1:n.1819+2501G= | |
NM_018058.7:c.1819+2501G= MANE Select | NP_060528.3:n.1819+2501G= |