HGVS | Genome Assembly |
---|---|
NC_000005.10:g.177993040A>T , CM000667.2:g.177993040A>T | GRCh38 |
NC_000005.9:g.177420041A>T , CM000667.1:g.177420041A>T | GRCh37 |
NC_000005.8:g.177352647A>T | NCBI36 |
NG_015889.1:g.8203T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000308304.2:c.350T>A MANE Select | ENSP00000311290.2:p.Phe117Tyr | |
NM_006261.4:c.350T>A | NP_006252.3:p.Phe117Tyr | |
NM_006261.5:c.350T>A MANE Select | NP_006252.4:p.Phe117Tyr |