HGVS | Genome Assembly |
---|---|
NC_000019.10:g.6713227T>G , CM000681.2:g.6713227T>G | GRCh38 |
NC_000019.9:g.6713238T>G , CM000681.1:g.6713238T>G | GRCh37 |
NC_000019.8:g.6664238T>G | NCBI36 |
NG_009557.1:g.12425A>C , LRG_27:g.12425A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695652.1:c.842A>C | ENSP00000512083.1:p.Lys281Thr | |
ENST00000695654.1:c.89A>C | ENSP00000512085.1:p.Lys30Thr | |
ENST00000695692.1:n.289A>C | ||
ENST00000245907.11:c.965A>C MANE Select | ENSP00000245907.4:p.Lys322Thr | |
ENST00000245907.10:c.965A>C | ENSP00000245907.4:p.Lys322Thr | |
ENST00000594270.5:n.89A>C | ||
ENST00000595577.1:n.469A>C | ||
ENST00000597442.5:n.215A>C | ||
NM_000064.3:c.965A>C | NP_000055.2:p.Lys322Thr | |
NM_000064.4:c.965A>C MANE Select | NP_000055.2:p.Lys322Thr |