HGVS | Genome Assembly |
---|---|
NC_000005.10:g.136046402G= , CM000667.2:g.136046402G= | GRCh38 |
NC_000005.9:g.135382091G= , CM000667.1:g.135382091G= | GRCh37 |
NC_000005.8:g.135409990G= | NCBI36 |
NG_012646.1:g.22508G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000442011.7:c.366G= MANE Select | ENSP00000416330.2:p.Thr122= | |
ENST00000442011.6:c.366G= | ENSP00000416330.2:p.Thr122= | |
ENST00000504185.5:n.523G= | ||
ENST00000506699.5:n.431G= | ||
ENST00000507018.5:c.283G= | ||
ENST00000515433.1:n.658G= | ||
NM_000358.2:c.366G= | NP_000349.1:p.Thr122= | |
NM_000358.3:c.366G= MANE Select | NP_000349.1:p.Thr122= |