Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32443374T= , CM000668.2:g.32443374T= | GRCh38 |
| NC_000006.11:g.32411151T= , CM000668.1:g.32411151T= | GRCh37 |
| NC_000006.10:g.32519129T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000395388.7:c.518T= MANE Select | ENSP00000378786.2:p.Phe173= | |
| ENST00000374982.5:c.443T= | ENSP00000364121.5:p.Phe148= | |
| ENST00000395388.6:c.518T= | ENSP00000378786.2:p.Phe173= | |
| NM_019111.4:c.518T= | NP_061984.2:p.Phe173= | |
| NM_019111.5:c.518T= MANE Select | NP_061984.2:p.Phe173= |