Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.6713260A= , CM000681.2:g.6713260A= | GRCh38 |
| NC_000019.9:g.6713271A= , CM000681.1:g.6713271A= | GRCh37 |
| NC_000019.8:g.6664271A= | NCBI36 |
| NG_009557.1:g.12392T= , LRG_27:g.12392T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695652.1:c.809T= | ENSP00000512083.1:p.Val270= | |
| ENST00000695654.1:c.56T= | ENSP00000512085.1:p.Val19= | |
| ENST00000695692.1:n.256T= | ||
| ENST00000245907.11:c.932T= MANE Select | ENSP00000245907.4:p.Val311= | |
| ENST00000245907.10:c.932T= | ENSP00000245907.4:p.Val311= | |
| ENST00000594270.5:n.56T= | ||
| ENST00000595577.1:n.436T= | ||
| ENST00000597442.5:n.182T= | ||
| NM_000064.3:c.932T= | NP_000055.2:p.Val311= | |
| NM_000064.4:c.932T= MANE Select | NP_000055.2:p.Val311= |