Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.160139786T= , CM000663.2:g.160139786T= | GRCh38 |
| NC_000001.10:g.160109576T= , CM000663.1:g.160109576T= | GRCh37 |
| NC_000001.9:g.158376200T= | NCBI36 |
| NG_008014.1:g.29029T= , LRG_6:g.29029T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361216.8:c.2942+45T= MANE Select | ENSP00000354490.3:n.2942+45T= | |
| ENST00000361216.7:c.2942+45T= | ENSP00000354490.3:n.2942+45T= | |
| ENST00000392233.7:c.2942+45T= | ENSP00000376066.3:n.2942+45T= | |
| ENST00000447527.1:c.2023+45T= | ||
| ENST00000463989.1:n.278+45T= | ||
| NM_000702.3:c.2942+45T= | NP_000693.1:n.2942+45T= | |
| NM_000702.4:c.2942+45T= MANE Select | NP_000693.1:n.2942+45T= |