Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.47283176A= , CM000679.2:g.47283176A= | GRCh38 |
| NC_000017.10:g.45360542A= , CM000679.1:g.45360542A= | GRCh37 |
| NC_000017.9:g.42715541A= | NCBI36 |
| NG_008332.2:g.34335A= , LRG_481:g.34335A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696963.1:c.166-178A= | ENSP00000513002.1:n.166-178A= | |
| ENST00000559488.7:c.166-178A= MANE Select | ENSP00000452786.2:n.166-178A= | |
| ENST00000559488.5:c.166-178A= | ENSP00000452786.1:n.166-178A= | |
| ENST00000560629.1:c.131-178A= | ||
| ENST00000571680.1:c.166-178A= | ENSP00000461626.1:n.166-178A= | |
| NM_000212.2:c.166-178A= , LRG_481t1:c.166-178A= | NP_000203.2:n.166-178A= | |
| NM_000212.3:c.166-178A= MANE Select | NP_000203.2:n.166-178A= |