HGVS | Genome Assembly |
---|---|
NC_000005.10:g.136046387C>G , CM000667.2:g.136046387C>G | GRCh38 |
NC_000005.9:g.135382076C>G , CM000667.1:g.135382076C>G | GRCh37 |
NC_000005.8:g.135409975C>G | NCBI36 |
NG_012646.1:g.22493C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000442011.7:c.351C>G MANE Select | ENSP00000416330.2:p.Thr117= | |
ENST00000442011.6:c.351C>G | ENSP00000416330.2:p.Thr117= | |
ENST00000504185.5:n.508C>G | ||
ENST00000506699.5:n.416C>G | ||
ENST00000507018.5:c.268C>G | ||
ENST00000515433.1:n.643C>G | ||
NM_000358.2:c.351C>G | NP_000349.1:p.Thr117= | |
NM_000358.3:c.351C>G MANE Select | NP_000349.1:p.Thr117= |