HGVS | Genome Assembly |
---|---|
NC_000007.14:g.98186920G= , CM000669.2:g.98186920G= | GRCh38 |
NC_000007.13:g.97816232G= , CM000669.1:g.97816232G= | GRCh37 |
NC_000007.12:g.97654168G= | NCBI36 |
NG_013375.1:g.85036G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000297293.6:c.920G= MANE Select | ENSP00000297293.5:p.Arg307= | |
ENST00000297293.5:c.920G= | ENSP00000297293.5:p.Arg307= | |
NM_014916.3:c.920G= | NP_055731.2:p.Arg307= | |
XM_011515981.1:c.914G= | XP_011514283.1:p.Arg305= | |
XM_011515981.3:c.914G= | XP_011514283.1:p.Arg305= | |
NM_014916.4:c.920G= MANE Select | NP_055731.2:p.Arg307= |