Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.215998848A= , CM000663.2:g.215998848A= | GRCh38 |
| NC_000001.10:g.216172190A= , CM000663.1:g.216172190A= | GRCh37 |
| NC_000001.9:g.214238813A= | NCBI36 |
| NG_009497.1:g.429549T= | |
| NG_009497.2:g.429601T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307340.8:c.6657+39T= MANE Select | ENSP00000305941.3:n.6657+39T= | |
| ENST00000674083.1:c.6657+39T= | ENSP00000501296.1:n.6657+39T= | |
| ENST00000307340.7:c.6657+39T= | ENSP00000305941.3:n.6657+39T= | |
| NM_206933.2:c.6657+39T= | NP_996816.2:n.6657+39T= | |
| NM_206933.3:c.6657+39T= | NP_996816.2:n.6657+39T= | |
| NM_206933.4:c.6657+39T= MANE Select | NP_996816.3:n.6657+39T= |