Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.21174701C= , CM000674.2:g.21174701C= | GRCh38 |
| NC_000012.11:g.21327635C= , CM000674.1:g.21327635C= | GRCh37 |
| NC_000012.10:g.21218902C= | NCBI36 |
| NG_011745.1:g.48508C= , LRG_1022:g.48508C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000256958.3:c.351C= MANE Select | ENSP00000256958.2:p.Phe117= | |
| ENST00000256958.2:c.351C= | ENSP00000256958.2:p.Phe117= | |
| ENST00000543498.5:c.426-2075C= | ||
| NM_006446.4:c.351C= , LRG_1022t1:c.351C= | NP_006437.3:p.Phe117= | |
| NM_006446.5:c.351C= MANE Select | NP_006437.3:p.Phe117= |