HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133353797G>A , CM000671.2:g.133353797G>A | GRCh38 |
NC_000009.10:g.135210473G>A | NCBI36 |
NG_008477.1:g.7710C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000371974.8:c.467C>T MANE Select | ENSP00000361042.3:p.Thr156Ile | |
ENST00000371974.7:c.467C>T | ENSP00000361042.3:p.Thr156Ile | |
ENST00000437995.1:n.413C>T | ||
ENST00000495952.5:n.457C>T | ||
ENST00000615505.4:c.140C>T | ENSP00000482067.1:p.Thr47Ile | |
NM_001280787.1:c.140C>T | NP_001267716.1:p.Thr47Ile | |
NM_003172.3:c.467C>T | NP_003163.1:p.Thr156Ile | |
XM_011518942.1:c.140C>T | XP_011517244.1:p.Thr47Ile | |
NM_003172.4:c.467C>T MANE Select | NP_003163.1:p.Thr156Ile |