HGVS | Genome Assembly |
---|---|
NC_000005.10:g.128395191A>T , CM000667.2:g.128395191A>T | GRCh38 |
NC_000005.9:g.127730884A>T , CM000667.1:g.127730884A>T | GRCh37 |
NC_000005.8:g.127758783A>T | NCBI36 |
NG_008750.1:g.147852T>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000703787.1:n.869T>A | ||
ENST00000262464.9:c.1162T>A MANE Select | ENSP00000262464.4:p.Cys388Ser | |
ENST00000262464.8:c.1162T>A | ENSP00000262464.4:p.Cys388Ser | |
ENST00000508053.5:c.1162T>A | ENSP00000424571.1:p.Cys388Ser | |
ENST00000508989.5:c.1063T>A | ENSP00000425596.1:p.Cys355Ser | |
ENST00000619499.4:c.1159T>A | ENSP00000482132.1:p.Cys387Ser | |
NM_001999.3:c.1162T>A | NP_001990.2:p.Cys388Ser | |
XM_017009228.2:c.1079-1823T>A | XP_016864717.1:n.1079-1823T>A | |
NM_001999.4:c.1162T>A MANE Select | NP_001990.2:p.Cys388Ser |