HGVS | Genome Assembly |
---|---|
NC_000005.10:g.148827675T>G , CM000667.2:g.148827675T>G | GRCh38 |
NC_000005.9:g.148207238T>G , CM000667.1:g.148207238T>G | GRCh37 |
NC_000005.8:g.148187431T>G | NCBI36 |
NG_016421.1:g.6083T>G | |
NG_016421.2:g.6083T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000305988.6:c.844T>G MANE Select | ENSP00000305372.4:p.Phe282Val | |
ENST00000305988.5:c.844T>G | ENSP00000305372.4:p.Phe282Val | |
NM_000024.5:c.844T>G | NP_000015.1:p.Phe282Val | |
NM_000024.6:c.844T>G MANE Select | NP_000015.2:p.Phe282Val |