Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.48981411C>T , CM000674.2:g.48981411C>T | GRCh38 |
| NC_000012.11:g.49375194C>T , CM000674.1:g.49375194C>T | GRCh37 |
| NC_000012.10:g.47661461C>T | NCBI36 |
| NG_033141.1:g.7959C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005430.4:c.884C>T MANE Select | NP_005421.1:p.Ser295Leu |
| ENST00000293549.4:c.884C>T MANE Select | ENSP00000293549.3:p.Ser295Leu |
| NM_005430.3:c.884C>T | NP_005421.1:p.Ser295Leu |
| ENST00000293549.3:c.884C>T | ENSP00000293549.3:p.Ser295Leu |
| ENST00000613114.4:c.851C>T | ENSP00000481240.1:p.Ser284Leu |