HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133352761G= , CM000671.2:g.133352761G= | GRCh38 |
NC_000009.10:g.135209437G= | NCBI36 |
NG_008477.1:g.8746C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000371974.8:c.521C= MANE Select | ENSP00000361042.3:p.Thr174= | |
ENST00000371974.7:c.521C= | ENSP00000361042.3:p.Thr174= | |
ENST00000437995.1:n.462-31C= | ||
ENST00000495952.5:n.511C= | ||
ENST00000615505.4:c.194C= | ENSP00000482067.1:p.Thr65= | |
NM_001280787.1:c.194C= | NP_001267716.1:p.Thr65= | |
NM_003172.3:c.521C= | NP_003163.1:p.Thr174= | |
XM_011518942.1:c.194C= | XP_011517244.1:p.Thr65= | |
NM_003172.4:c.521C= MANE Select | NP_003163.1:p.Thr174= |