HGVS | Genome Assembly |
---|---|
NC_000001.11:g.17024028C>A , CM000663.2:g.17024028C>A | GRCh38 |
NC_000001.10:g.17350523C>A , CM000663.1:g.17350523C>A | GRCh37 |
NC_000001.9:g.17223110C>A | NCBI36 |
NG_012340.1:g.35143G>T , LRG_316:g.35143G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000463045.3:c.416G>T | ENSP00000481376.2:p.Cys139Phe | |
ENST00000491274.6:c.545G>T | ENSP00000480482.2:p.Cys182Phe | |
ENST00000375499.8:c.587G>T MANE Select | ENSP00000364649.3:p.Cys196Phe | |
ENST00000375499.7:c.587G>T | ENSP00000364649.3:p.Cys196Phe | |
ENST00000485515.5:n.521G>T | ||
ENST00000491274.5:c.545G>T | ENSP00000480482.1:p.Cys182Phe | |
NM_003000.2:c.587G>T , LRG_316t1:c.587G>T | NP_002991.2:p.Cys196Phe | |
NM_003000.3:c.587G>T MANE Select | NP_002991.2:p.Cys196Phe |