Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.81478465A= , CM000670.2:g.81478465A= | GRCh38 |
| NC_000008.10:g.82390700A= , CM000670.1:g.82390700A= | GRCh37 |
| NC_000008.9:g.82553255A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000256104.5:c.*400T= MANE Select | ENSP00000256104.4:n.*400T= | |
| ENST00000256104.4:c.*400T= | ENSP00000256104.4:n.*400T= | |
| XR_001745980.1:n.514+16491A= | ||
| NM_001442.3:c.*400T= MANE Select | NP_001433.1:n.*400T= |