Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.17022939A= , CM000663.2:g.17022939A= | GRCh38 |
| NC_000001.10:g.17349434A= , CM000663.1:g.17349434A= | GRCh37 |
| NC_000001.9:g.17222021A= | NCBI36 |
| NG_012340.1:g.36232T= , LRG_316:g.36232T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000463045.3:c.472-209T= | ENSP00000481376.2:n.472-209T= | |
| ENST00000491274.6:c.601-209T= | ENSP00000480482.2:n.601-209T= | |
| ENST00000375499.8:c.643-209T= MANE Select | ENSP00000364649.3:n.643-209T= | |
| ENST00000375499.7:c.643-209T= | ENSP00000364649.3:n.643-209T= | |
| ENST00000475049.5:n.67+155T= | ||
| ENST00000485092.5:n.98T= | ||
| ENST00000485515.5:n.577-209T= | ||
| NM_003000.2:c.643-209T= , LRG_316t1:c.643-209T= | NP_002991.2:n.643-209T= | |
| NM_003000.3:c.643-209T= MANE Select | NP_002991.2:n.643-209T= |