HGVS | Genome Assembly |
---|---|
NC_000001.11:g.160881998T>C , CM000663.2:g.160881998T>C | GRCh38 |
NC_000001.10:g.160851788T>C , CM000663.1:g.160851788T>C | GRCh37 |
NC_000001.9:g.159118412T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000326245.4:c.364A>G MANE Select | ENSP00000323587.3:p.Thr122Ala | |
ENST00000326245.3:c.364A>G | ENSP00000323587.3:p.Thr122Ala | |
ENST00000464077.1:n.298A>G | ||
NM_017625.2:c.364A>G | NP_060095.2:p.Thr122Ala | |
NM_017625.3:c.364A>G MANE Select | NP_060095.2:p.Thr122Ala |