HGVS | Genome Assembly |
---|---|
NC_000005.10:g.136046355T= , CM000667.2:g.136046355T= | GRCh38 |
NC_000005.9:g.135382044T= , CM000667.1:g.135382044T= | GRCh37 |
NC_000005.8:g.135409943T= | NCBI36 |
NG_012646.1:g.22461T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000442011.7:c.319T= MANE Select | ENSP00000416330.2:p.Tyr107= | |
ENST00000442011.6:c.319T= | ENSP00000416330.2:p.Tyr107= | |
ENST00000504185.5:n.476T= | ||
ENST00000506699.5:n.384T= | ||
ENST00000507018.5:c.236T= | ||
ENST00000515433.1:n.611T= | ||
NM_000358.2:c.319T= | NP_000349.1:p.Tyr107= | |
NM_000358.3:c.319T= MANE Select | NP_000349.1:p.Tyr107= |