Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5226635A>G , CM000673.2:g.5226635A>G | GRCh38 |
| NC_000011.9:g.5247865A>G , CM000673.1:g.5247865A>G | GRCh37 |
| NC_000011.8:g.5204441A>G | NCBI36 |
| NG_000007.3:g.70981T>C | |
| NG_059281.1:g.5437T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000518.5:c.257T>C MANE Select | NP_000509.1:p.Phe86Ser |
| ENST00000335295.4:c.257T>C MANE Select | ENSP00000333994.3:p.Phe86Ser |
| NM_000518.4:c.257T>C | NP_000509.1:p.Phe86Ser |
| ENST00000380315.2:c.257T>C | ENSP00000369671.2:p.Phe86Ser |
| ENST00000475226.1:n.189T>C | |
| ENST00000485743.1:n.308T>C | |
| ENST00000633227.1:c.*73T>C | ENSP00000488004.1:n.*73T>C |
| ENST00000647020.1:c.257T>C | ENSP00000494175.1:p.Phe86Ser |