HGVS | Genome Assembly |
---|---|
NC_000023.11:g.136659270C>A , CM000685.2:g.136659270C>A | GRCh38 |
NC_000023.10:g.135741429C>A , CM000685.1:g.135741429C>A | GRCh37 |
NC_000023.9:g.135569095C>A | NCBI36 |
NG_007280.1:g.16094C>A , LRG_141:g.16094C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695724.1:c.*259C>A | ENSP00000512122.1:n.*259C>A | |
ENST00000695725.1:c.*196C>A | ENSP00000512123.1:n.*196C>A | |
ENST00000695726.1:n.2609C>A | ||
ENST00000695729.1:n.3444C>A | ||
ENST00000370629.7:c.641C>A MANE Select | ENSP00000359663.2:p.Ser214Tyr | |
ENST00000370628.2:c.578C>A | ENSP00000359662.2:p.Ser193Tyr | |
ENST00000370629.6:c.641C>A | ENSP00000359663.2:p.Ser214Tyr | |
NM_000074.2:c.641C>A , LRG_141t1:c.641C>A | NP_000065.1:p.Ser214Tyr | |
NM_000074.3:c.641C>A MANE Select | NP_000065.1:p.Ser214Tyr |