Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.215782470A= , CM000663.2:g.215782470A= | GRCh38 |
| NC_000001.10:g.215955812A= , CM000663.1:g.215955812A= | GRCh37 |
| NC_000001.9:g.214022435A= | NCBI36 |
| NG_009497.1:g.645927T= | |
| NG_009497.2:g.645979T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307340.8:c.10585+268T= MANE Select | ENSP00000305941.3:n.10585+268T= | |
| ENST00000674083.1:c.10585+268T= | ENSP00000501296.1:n.10585+268T= | |
| ENST00000307340.7:c.10585+268T= | ENSP00000305941.3:n.10585+268T= | |
| NM_206933.2:c.10585+268T= | NP_996816.2:n.10585+268T= | |
| NM_206933.3:c.10585+268T= | NP_996816.2:n.10585+268T= | |
| NM_206933.4:c.10585+268T= MANE Select | NP_996816.3:n.10585+268T= |