HGVS | Genome Assembly |
---|---|
NC_000007.14:g.98186926C>T , CM000669.2:g.98186926C>T | GRCh38 |
NC_000007.13:g.97816238C>T , CM000669.1:g.97816238C>T | GRCh37 |
NC_000007.12:g.97654174C>T | NCBI36 |
NG_013375.1:g.85042C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000297293.6:c.926C>T MANE Select | ENSP00000297293.5:p.Thr309Ile | |
ENST00000297293.5:c.926C>T | ENSP00000297293.5:p.Thr309Ile | |
NM_014916.3:c.926C>T | NP_055731.2:p.Thr309Ile | |
XM_011515981.1:c.920C>T | XP_011514283.1:p.Thr307Ile | |
XM_011515981.3:c.920C>T | XP_011514283.1:p.Thr307Ile | |
NM_014916.4:c.926C>T MANE Select | NP_055731.2:p.Thr309Ile |