Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32443366C= , CM000668.2:g.32443366C= | GRCh38 |
| NC_000006.11:g.32411143C= , CM000668.1:g.32411143C= | GRCh37 |
| NC_000006.10:g.32519121C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000395388.7:c.510C= MANE Select | ENSP00000378786.2:p.Phe170= | |
| ENST00000374982.5:c.435C= | ENSP00000364121.5:p.Phe145= | |
| ENST00000395388.6:c.510C= | ENSP00000378786.2:p.Phe170= | |
| NM_019111.4:c.510C= | NP_061984.2:p.Phe170= | |
| NM_019111.5:c.510C= MANE Select | NP_061984.2:p.Phe170= |