Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.5044947T= , CM000674.2:g.5044947T= | GRCh38 |
| NC_000012.11:g.5154113T= , CM000674.1:g.5154113T= | GRCh37 |
| NC_000012.10:g.5024374T= | NCBI36 |
| NG_012198.1:g.6029T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252321.5:c.800T= MANE Select | ENSP00000252321.3:p.Phe267= | |
| ENST00000252321.4:c.800T= | ENSP00000252321.3:p.Phe267= | |
| NM_002234.3:c.800T= | NP_002225.2:p.Phe267= | |
| NM_002234.4:c.800T= MANE Select | NP_002225.2:p.Phe267= |