HGVS | Genome Assembly |
---|---|
NC_000004.12:g.41745896A>C , CM000666.2:g.41745896A>C | GRCh38 |
NC_000004.11:g.41747913A>C , CM000666.1:g.41747913A>C | GRCh37 |
NC_000004.10:g.41442670A>C | NCBI36 |
NG_008243.1:g.8075T>G , LRG_513:g.8075T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000226382.4:c.856T>G MANE Select | ENSP00000226382.2:p.Ser286Ala | |
ENST00000226382.3:c.856T>G | ENSP00000226382.2:p.Ser286Ala | |
NM_003924.3:c.856T>G , LRG_513t1:c.856T>G | NP_003915.2:p.Ser286Ala | |
NM_003924.4:c.856T>G MANE Select | NP_003915.2:p.Ser286Ala |