Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.173535G= , CM000678.2:g.173535G= | GRCh38 |
| NC_000016.9:g.223534G= , CM000678.1:g.223534G= | GRCh37 |
| NC_000016.8:g.163534G= | NCBI36 |
| NG_000006.1:g.34398G= | |
| NG_059186.1:g.1885G= | |
| NG_059271.1:g.5689G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000251595.11:c.364G= MANE Select | ENSP00000251595.6:p.Val122= | |
| ENST00000251595.10:c.364G= | ENSP00000251595.6:p.Val122= | |
| ENST00000397806.1:c.268G= | ENSP00000380908.1:p.Val90= | |
| ENST00000482565.1:n.500G= | ||
| NM_000517.4:c.364G= | NP_000508.1:p.Val122= | |
| NM_000517.6:c.364G= MANE Select | NP_000508.1:p.Val122= |