HGVS | Genome Assembly |
---|---|
NC_000019.10:g.6713279T>G , CM000681.2:g.6713279T>G | GRCh38 |
NC_000019.9:g.6713290T>G , CM000681.1:g.6713290T>G | GRCh37 |
NC_000019.8:g.6664290T>G | NCBI36 |
NG_009557.1:g.12373A>C , LRG_27:g.12373A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695652.1:c.790A>C | ENSP00000512083.1:p.Lys264Gln | |
ENST00000695654.1:c.37A>C | ENSP00000512085.1:p.Lys13Gln | |
ENST00000695692.1:n.237A>C | ||
ENST00000245907.11:c.913A>C MANE Select | ENSP00000245907.4:p.Lys305Gln | |
ENST00000245907.10:c.913A>C | ENSP00000245907.4:p.Lys305Gln | |
ENST00000594270.5:n.37A>C | ||
ENST00000595577.1:n.417A>C | ||
ENST00000597442.5:n.163A>C | ||
NM_000064.3:c.913A>C | NP_000055.2:p.Lys305Gln | |
NM_000064.4:c.913A>C MANE Select | NP_000055.2:p.Lys305Gln |