HGVS | Genome Assembly |
---|---|
NC_000018.10:g.31598638A>T , CM000680.2:g.31598638A>T | GRCh38 |
NC_000018.9:g.29178601A>T , CM000680.1:g.29178601A>T | GRCh37 |
NC_000018.8:g.27432599A>T | NCBI36 |
NG_009490.1:g.11872A>T , LRG_416:g.11872A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000237014.8:c.407A>T MANE Select | ENSP00000237014.4:p.Tyr136Phe | |
ENST00000610404.5:c.311A>T | ENSP00000477599.2:p.Tyr104Phe | |
ENST00000649620.1:c.407A>T | ENSP00000497927.1:p.Tyr136Phe | |
ENST00000237014.7:c.407A>T | ENSP00000237014.3:p.Tyr136Phe | |
ENST00000610404.4:c.521A>T | ENSP00000477599.1:p.Tyr174Phe | |
ENST00000613781.1:c.383A>T | ENSP00000479174.1:p.Tyr128Phe | |
NM_000371.3:c.407A>T , LRG_416t1:c.407A>T | NP_000362.1:p.Tyr136Phe | |
NM_000371.4:c.407A>T MANE Select | NP_000362.1:p.Tyr136Phe |