HGVS | Genome Assembly |
---|---|
NC_000016.10:g.67940398A>G , CM000678.2:g.67940398A>G | GRCh38 |
NC_000016.9:g.67974301A>G , CM000678.1:g.67974301A>G | GRCh37 |
NC_000016.8:g.66531802A>G | NCBI36 |
NG_009778.1:g.8715T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264005.10:c.829T>C MANE Select | ENSP00000264005.5:p.Phe277Leu | |
ENST00000264005.9:c.829T>C | ENSP00000264005.5:p.Phe277Leu | |
ENST00000570369.5:c.156-324T>C | ||
ENST00000570980.1:c.613T>C | ENSP00000464651.1:p.Phe205Leu | |
ENST00000573538.5:c.567T>C | ENSP00000463220.1:n.567T>C | |
NM_000229.1:c.829T>C | NP_000220.1:p.Phe277Leu | |
NM_000229.2:c.829T>C MANE Select | NP_000220.1:p.Phe277Leu |