Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.45766980A= , CM000681.2:g.45766980A= | GRCh38 |
| NC_000019.9:g.46270238A= , CM000681.1:g.46270238A= | GRCh37 |
| NC_000019.8:g.50962078A= | NCBI36 |
| NG_012745.1:g.7260T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000317578.7:c.979T= MANE Select | ENSP00000316842.4:p.Phe327= | |
| ENST00000317578.6:c.979T= | ENSP00000316842.4:p.Phe327= | |
| ENST00000560160.1:c.587-869T= | ||
| ENST00000560168.1:c.*167T= | ENSP00000453189.2:n.*167T= | |
| ENST00000622857.1:c.16-1018T= | ENSP00000481365.1:n.16-1018T= | |
| NM_175875.4:c.979T= | NP_787071.2:p.Phe327= | |
| NM_175875.5:c.979T= MANE Select | NP_787071.3:p.Phe327= |