HGVS | Genome Assembly |
---|---|
NC_000019.10:g.6713239T>G , CM000681.2:g.6713239T>G | GRCh38 |
NC_000019.9:g.6713250T>G , CM000681.1:g.6713250T>G | GRCh37 |
NC_000019.8:g.6664250T>G | NCBI36 |
NG_009557.1:g.12413A>C , LRG_27:g.12413A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695652.1:c.830A>C | ENSP00000512083.1:p.Asp277Ala | |
ENST00000695654.1:c.77A>C | ENSP00000512085.1:p.Asp26Ala | |
ENST00000695692.1:n.277A>C | ||
ENST00000245907.11:c.953A>C MANE Select | ENSP00000245907.4:p.Asp318Ala | |
ENST00000245907.10:c.953A>C | ENSP00000245907.4:p.Asp318Ala | |
ENST00000594270.5:n.77A>C | ||
ENST00000595577.1:n.457A>C | ||
ENST00000597442.5:n.203A>C | ||
NM_000064.3:c.953A>C | NP_000055.2:p.Asp318Ala | |
NM_000064.4:c.953A>C MANE Select | NP_000055.2:p.Asp318Ala |