Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.38682782T= , CM000668.2:g.38682782T= | GRCh38 |
| NC_000006.11:g.38650558T= , CM000668.1:g.38650558T= | GRCh37 |
| NC_000006.10:g.38758536T= | NCBI36 |
| NG_012074.1:g.25395A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373365.5:c.376+26A= MANE Select | ENSP00000362463.3:n.376+26A= | |
| ENST00000373365.4:c.376+26A= | ENSP00000362463.3:n.376+26A= | |
| ENST00000470973.1:n.408+26A= | ||
| NM_006708.2:c.376+26A= | NP_006699.2:n.376+26A= | |
| NM_006708.3:c.376+26A= MANE Select | NP_006699.2:n.376+26A= |