Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.173228C= , CM000678.2:g.173228C= | GRCh38 |
| NC_000016.9:g.223227C= , CM000678.1:g.223227C= | GRCh37 |
| NC_000016.8:g.163227C= | NCBI36 |
| NG_000006.1:g.34091C= | |
| NG_059186.1:g.1578C= | |
| NG_059271.1:g.5382C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000251595.11:c.199C= MANE Select | ENSP00000251595.6:p.Leu67= | |
| ENST00000251595.10:c.199C= | ENSP00000251595.6:p.Leu67= | |
| ENST00000397806.1:c.103C= | ENSP00000380908.1:p.Leu35= | |
| ENST00000482565.1:n.335C= | ||
| ENST00000484216.1:n.168C= | ||
| NM_000517.4:c.199C= | NP_000508.1:p.Leu67= | |
| NM_000517.6:c.199C= MANE Select | NP_000508.1:p.Leu67= |