HGVS | Genome Assembly |
---|---|
NC_000001.11:g.160882033T>G , CM000663.2:g.160882033T>G | GRCh38 |
NC_000001.10:g.160851823T>G , CM000663.1:g.160851823T>G | GRCh37 |
NC_000001.9:g.159118447T>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000326245.4:c.329A>C MANE Select | ENSP00000323587.3:p.Tyr110Ser | |
ENST00000326245.3:c.329A>C | ENSP00000323587.3:p.Tyr110Ser | |
ENST00000464077.1:n.263A>C | ||
NM_017625.2:c.329A>C | NP_060095.2:p.Tyr110Ser | |
NM_017625.3:c.329A>C MANE Select | NP_060095.2:p.Tyr110Ser |