HGVS | Genome Assembly |
---|---|
NC_000008.11:g.18400253T>G , CM000670.2:g.18400253T>G | GRCh38 |
NC_000008.10:g.18257763T>G , CM000670.1:g.18257763T>G | GRCh37 |
NC_000008.9:g.18302043T>G | NCBI36 |
NG_012246.1:g.14009T>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000286479.4:c.250T>G MANE Select | ENSP00000286479.3:p.Phe84Val | |
ENST00000286479.3:c.250T>G | ENSP00000286479.3:p.Phe84Val | |
ENST00000520116.1:c.-57-84T>G | ENSP00000428416.1:n.-57-84T>G | |
NM_000015.2:c.250T>G | NP_000006.2:p.Phe84Val | |
XM_011544358.1:c.250T>G | XP_011542660.1:p.Phe84Val | |
XM_017012938.1:c.250T>G | XP_016868427.1:p.Phe84Val | |
NM_000015.3:c.250T>G MANE Select | NP_000006.2:p.Phe84Val |