Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94000866C>G , CM000663.2:g.94000866C>G | GRCh38 |
| NC_000001.10:g.94466422C>G , CM000663.1:g.94466422C>G | GRCh37 |
| NC_000001.9:g.94239010C>G | NCBI36 |
| NG_009073.1:g.125284G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.6449G>C MANE Select | ENSP00000359245.3:p.Cys2150Ser | |
| ENST00000370225.3:c.6449G>C | ENSP00000359245.3:p.Cys2150Ser | |
| ENST00000536513.5:c.2825G>C | ENSP00000439707.2:p.Cys942Ser | |
| NM_000350.2:c.6449G>C | NP_000341.2:p.Cys2150Ser | |
| NM_000350.3:c.6449G>C MANE Select | NP_000341.2:p.Cys2150Ser |