Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.5603514T= , CM000669.2:g.5603514T= | GRCh38 |
| NC_000007.13:g.5643145T= , CM000669.1:g.5643145T= | GRCh37 |
| NC_000007.12:g.5609671T= | NCBI36 |
| NG_030004.1:g.15710T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_003088.4:c.1008T= MANE Select | NP_003079.1:p.Phe336= |
| ENST00000382361.8:c.1008T= MANE Select | ENSP00000371798.3:p.Phe336= |
| NM_003088.3:c.1008T= | NP_003079.1:p.Phe336= |
| ENST00000382361.7:c.1008T= | ENSP00000371798.3:p.Phe336= |
| ENST00000405801.2:c.174T= | ENSP00000383982.2:p.Phe58= |
| ENST00000444748.5:c.174T= | ENSP00000404506.1:p.Phe58= |
| ENST00000447103.5:c.174T= | ENSP00000409967.1:p.Phe58= |
| ENST00000473330.1:n.561T= |