HGVS | Genome Assembly |
---|---|
NC_000004.12:g.177439683G>A , CM000666.2:g.177439683G>A | GRCh38 |
NC_000004.11:g.178360837G>A , CM000666.1:g.178360837G>A | GRCh37 |
NC_000004.10:g.178597831G>A | NCBI36 |
NG_011845.2:g.7821C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264595.7:c.287C>T MANE Select | ENSP00000264595.2:p.Thr96Ile | |
ENST00000264595.6:c.287C>T | ENSP00000264595.2:p.Thr96Ile | |
ENST00000506853.5:n.321C>T | ||
ENST00000510955.5:n.315+590C>T | ||
NM_000027.3:c.287C>T | NP_000018.2:p.Thr96Ile | |
NM_001171988.1:c.287C>T | NP_001165459.1:p.Thr96Ile | |
NR_033655.1:n.415C>T | ||
XM_006714123.2:c.287C>T | XP_006714186.1:p.Thr96Ile | |
XR_001741155.2:n.381C>T | ||
NM_000027.4:c.287C>T MANE Select | NP_000018.2:p.Thr96Ile | |
NM_001171988.2:c.287C>T | NP_001165459.1:p.Thr96Ile | |
NR_033655.2:n.349C>T |