Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154997050A= , CM000685.2:g.154997050A= | GRCh38 |
| NC_000023.10:g.154225325A= , CM000685.1:g.154225325A= | GRCh37 |
| NC_000023.9:g.153878519A= | NCBI36 |
| NG_011403.1:g.30674T= | |
| NG_011403.2:g.30674T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.311T= MANE Select | ENSP00000353393.4:p.Val104= | |
| ENST00000647125.1:c.*97T= | ENSP00000496062.1:n.*97T= | |
| ENST00000360256.8:c.311T= | ENSP00000353393.4:p.Val104= | |
| ENST00000423959.5:c.206T= | ENSP00000409446.1:p.Val69= | |
| ENST00000453950.1:c.293T= | ENSP00000389153.1:p.Val98= | |
| NM_000132.3:c.311T= | NP_000123.1:p.Val104= | |
| XM_011531126.1:c.206T= | XP_011529428.1:p.Val69= | |
| NM_000132.4:c.311T= MANE Select | NP_000123.1:p.Val104= |