HGVS | Genome Assembly |
---|---|
NC_000007.14:g.98187301T= , CM000669.2:g.98187301T= | GRCh38 |
NC_000007.13:g.97816613T= , CM000669.1:g.97816613T= | GRCh37 |
NC_000007.12:g.97654549T= | NCBI36 |
NG_013375.1:g.85417T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000297293.6:c.998+303T= MANE Select | ENSP00000297293.5:n.998+303T= | |
ENST00000297293.5:c.998+303T= | ENSP00000297293.5:n.998+303T= | |
NM_014916.3:c.998+303T= | NP_055731.2:n.998+303T= | |
XM_011515981.1:c.992+303T= | XP_011514283.1:n.992+303T= | |
XM_011515981.3:c.992+303T= | XP_011514283.1:n.992+303T= | |
NM_014916.4:c.998+303T= MANE Select | NP_055731.2:n.998+303T= |