Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.81478628C= , CM000670.2:g.81478628C= | GRCh38 |
| NC_000008.10:g.82390863C= , CM000670.1:g.82390863C= | GRCh37 |
| NC_000008.9:g.82553418C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000256104.5:c.*237G= MANE Select | ENSP00000256104.4:n.*237G= | |
| ENST00000256104.4:c.*237G= | ENSP00000256104.4:n.*237G= | |
| NM_001442.2:c.*237G= | NP_001433.1:n.*237G= | |
| XR_001745980.1:n.514+16654C= | ||
| NM_001442.3:c.*237G= MANE Select | NP_001433.1:n.*237G= |