HGVS | Genome Assembly |
---|---|
NC_000010.11:g.92645443T>C , CM000672.2:g.92645443T>C | GRCh38 |
NC_000010.10:g.94405200T>C , CM000672.1:g.94405200T>C | GRCh37 |
NC_000010.9:g.94395180T>C | NCBI36 |
NG_032580.1:g.57376T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000260731.5:c.2348T>C MANE Select | ENSP00000260731.3:p.Leu783Pro | |
ENST00000676621.1:c.*866T>C | ENSP00000503639.1:n.*866T>C | |
ENST00000676647.1:c.2141T>C | ENSP00000503394.1:p.Leu714Pro | |
ENST00000676757.1:c.2141T>C | ENSP00000504289.1:p.Leu714Pro | |
ENST00000677720.1:c.*322T>C | ENSP00000504840.1:n.*322T>C | |
ENST00000260731.4:c.2348T>C | ENSP00000260731.3:p.Leu783Pro | |
NM_004523.3:c.2348T>C | NP_004514.2:p.Leu783Pro | |
NM_004523.4:c.2348T>C MANE Select | NP_004514.2:p.Leu783Pro |