HGVS | Genome Assembly |
---|---|
NC_000005.10:g.128395187C>A , CM000667.2:g.128395187C>A | GRCh38 |
NC_000005.9:g.127730880C>A , CM000667.1:g.127730880C>A | GRCh37 |
NC_000005.8:g.127758779C>A | NCBI36 |
NG_008750.1:g.147856G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000703787.1:n.873G>T | ||
ENST00000262464.9:c.1166G>T MANE Select | ENSP00000262464.4:p.Cys389Phe | |
ENST00000262464.8:c.1166G>T | ENSP00000262464.4:p.Cys389Phe | |
ENST00000508053.5:c.1166G>T | ENSP00000424571.1:p.Cys389Phe | |
ENST00000508989.5:c.1067G>T | ENSP00000425596.1:p.Cys356Phe | |
ENST00000619499.4:c.1163G>T | ENSP00000482132.1:p.Cys388Phe | |
NM_001999.3:c.1166G>T | NP_001990.2:p.Cys389Phe | |
XM_017009228.2:c.1079-1819G>T | XP_016864717.1:n.1079-1819G>T | |
NM_001999.4:c.1166G>T MANE Select | NP_001990.2:p.Cys389Phe |