HGVS | Genome Assembly |
---|---|
NC_000019.10:g.6713200A>C , CM000681.2:g.6713200A>C | GRCh38 |
NC_000019.9:g.6713211A>C , CM000681.1:g.6713211A>C | GRCh37 |
NC_000019.8:g.6664211A>C | NCBI36 |
NG_009557.1:g.12452T>G , LRG_27:g.12452T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695652.1:c.869T>G | ENSP00000512083.1:p.Ile290Ser | |
ENST00000695654.1:c.116T>G | ENSP00000512085.1:p.Ile39Ser | |
ENST00000695692.1:n.316T>G | ||
ENST00000245907.11:c.992T>G MANE Select | ENSP00000245907.4:p.Ile331Ser | |
ENST00000245907.10:c.992T>G | ENSP00000245907.4:p.Ile331Ser | |
ENST00000594270.5:n.116T>G | ||
ENST00000595577.1:n.496T>G | ||
ENST00000597442.5:n.242T>G | ||
NM_000064.3:c.992T>G | NP_000055.2:p.Ile331Ser | |
NM_000064.4:c.992T>G MANE Select | NP_000055.2:p.Ile331Ser |