HGVS | Genome Assembly |
---|---|
NC_000017.11:g.42901061T>G , CM000679.2:g.42901061T>G | GRCh38 |
NC_000017.10:g.41053078T>G , CM000679.1:g.41053078T>G | GRCh37 |
NC_000017.9:g.38306604T>G | NCBI36 |
NG_011808.1:g.5264T>G , LRG_147:g.5264T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000253801.7:c.185T>G MANE Select | ENSP00000253801.1:p.Leu62Arg | |
ENST00000253801.6:c.185T>G | ENSP00000253801.1:p.Leu62Arg | |
ENST00000585489.1:c.185T>G | ENSP00000466202.1:p.Leu62Arg | |
ENST00000588481.1:n.250T>G | ||
ENST00000592383.5:c.185T>G | ENSP00000465958.1:p.Leu62Arg | |
NM_000151.3:c.185T>G | NP_000142.2:p.Leu62Arg | |
NM_001270397.1:c.185T>G | NP_001257326.1:p.Leu62Arg | |
NM_000151.4:c.185T>G MANE Select | NP_000142.2:p.Leu62Arg | |
NM_001270397.2:c.185T>G | NP_001257326.1:p.Leu62Arg |