Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154966663A= , CM000685.2:g.154966663A= | GRCh38 |
| NC_000023.10:g.154194938A= , CM000685.1:g.154194938A= | GRCh37 |
| NC_000023.9:g.153848132A= | NCBI36 |
| NG_011403.1:g.61061T= | |
| NG_011403.2:g.61061T= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000360256.9:c.1034T= MANE Select | ENSP00000353393.4:p.Val345= | |
| ENST00000647125.1:c.*910T= | ENSP00000496062.1:n.*910T= | |
| ENST00000360256.8:c.1034T= | ENSP00000353393.4:p.Val345= | |
| NM_000132.3:c.1034T= | NP_000123.1:p.Val345= | |
| XM_011531126.1:c.929T= | XP_011529428.1:p.Val310= | |
| NM_000132.4:c.1034T= MANE Select | NP_000123.1:p.Val345= |