HGVS | Genome Assembly |
---|---|
NC_000023.11:g.153741143G= , CM000685.2:g.153741143G= | GRCh38 |
NC_000023.10:g.153006597G= , CM000685.1:g.153006597G= | GRCh37 |
NC_000023.9:g.152659791G= | NCBI36 |
NG_009022.2:g.21276G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000218104.6:c.1780+424G= MANE Select | ENSP00000218104.3:n.1780+424G= | |
ENST00000218104.5:c.1780+424G= | ENSP00000218104.3:n.1780+424G= | |
NM_000033.3:c.1780+424G= | NP_000024.2:n.1780+424G= | |
XR_938507.1:n.2252+424G= | ||
XR_938507.2:n.2252+424G= | ||
NM_000033.4:c.1780+424G= MANE Select | NP_000024.2:n.1780+424G= |