Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.6587159A= , CM000671.2:g.6587159A= | GRCh38 |
| NC_000009.11:g.6587159A= , CM000671.1:g.6587159A= | GRCh37 |
| NC_000009.10:g.6577159A= | NCBI36 |
| NG_016397.1:g.63534T= , LRG_643:g.63534T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000170.3:c.1832T= MANE Select | NP_000161.2:p.Val611= |
| ENST00000321612.8:c.1832T= MANE Select | ENSP00000370737.4:p.Val611= |
| NM_000170.2:c.1832T= , LRG_643t1:c.1832T= | NP_000161.2:p.Val611= |
| ENST00000321612.6:c.1832T= | ENSP00000370737.3:p.Val611= |
| ENST00000639364.1:n.1532T= | |
| ENST00000639443.1:n.1400T= | |
| ENST00000639954.1:n.1540T= | |
| ENST00000640592.1:n.1715T= |