Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.3154697G= , CM000668.2:g.3154697G= | GRCh38 |
| NC_000006.11:g.3154931G= , CM000668.1:g.3154931G= | GRCh37 |
| NC_000006.10:g.3099930G= | NCBI36 |
| NG_042223.1:g.7853C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000333628.4:c.504C= MANE Select | ENSP00000369703.2:p.Ser168= | |
| ENST00000679400.1:n.560C= | ||
| ENST00000679907.1:n.892C= | ||
| ENST00000680036.1:n.1286C= | ||
| ENST00000680967.1:n.1594C= | ||
| ENST00000333628.3:c.504C= | ENSP00000369703.2:p.Ser168= | |
| ENST00000489942.1:n.699C= | ||
| NM_001069.2:c.504C= | NP_001060.1:p.Ser168= | |
| NM_001310315.1:c.249C= | NP_001297244.1:p.Ser83= | |
| NM_001069.3:c.504C= MANE Select | NP_001060.1:p.Ser168= | |
| NM_001310315.2:c.249C= | NP_001297244.1:p.Ser83= |