Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.173421C= , CM000678.2:g.173421C= | GRCh38 |
| NC_000016.9:g.223420C= , CM000678.1:g.223420C= | GRCh37 |
| NC_000016.8:g.163420C= | NCBI36 |
| NG_000006.1:g.34284C= | |
| NG_059186.1:g.1771C= | |
| NG_059271.1:g.5575C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000251595.11:c.301-51C= MANE Select | ENSP00000251595.6:n.301-51C= | |
| ENST00000251595.10:c.301-51C= | ENSP00000251595.6:n.301-51C= | |
| ENST00000397806.1:c.205-51C= | ENSP00000380908.1:n.205-51C= | |
| ENST00000482565.1:n.437-51C= | ||
| ENST00000484216.1:n.361C= | ||
| NM_000517.4:c.301-51C= | NP_000508.1:n.301-51C= | |
| NM_000517.6:c.301-51C= MANE Select | NP_000508.1:n.301-51C= |