HGVS | Genome Assembly |
---|---|
NC_000011.10:g.5226754A>G , CM000673.2:g.5226754A>G | GRCh38 |
NC_000011.9:g.5247984A>G , CM000673.1:g.5247984A>G | GRCh37 |
NC_000011.8:g.5204560A>G | NCBI36 |
NG_000007.3:g.70862T>C | |
NG_059281.1:g.5318T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000647020.1:c.138T>C | ENSP00000494175.1:p.Phe46= | |
ENST00000335295.4:c.138T>C MANE Select | ENSP00000333994.3:p.Phe46= | |
ENST00000380315.2:c.138T>C | ENSP00000369671.2:p.Phe46= | |
ENST00000475226.1:n.70T>C | ||
ENST00000485743.1:n.189T>C | ||
ENST00000633227.1:c.122T>C | ENSP00000488004.1:p.Leu41Ser | |
NM_000518.4:c.138T>C | NP_000509.1:p.Phe46= | |
NM_000518.5:c.138T>C MANE Select | NP_000509.1:p.Phe46= |