Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.98542019C= , CM000671.2:g.98542019C= | GRCh38 |
| NC_000009.11:g.101304301C= , CM000671.1:g.101304301C= | GRCh37 |
| NC_000009.10:g.100344122C= | NCBI36 |
| NG_016426.1:g.172179G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000259455.4:c.484G= MANE Select | ENSP00000259455.2:p.Val162= | |
| ENST00000637410.1:n.262G= | ||
| ENST00000637717.1:c.100G= | ENSP00000490789.1:p.Val34= | |
| ENST00000638001.1:n.94G= | ||
| ENST00000259455.3:c.484G= | ENSP00000259455.2:p.Val162= | |
| ENST00000477471.1:n.271G= | ||
| ENST00000634227.1:n.258G= | ||
| NM_005458.7:c.484G= | NP_005449.5:p.Val162= | |
| XM_017015331.2:c.190G= | XP_016870820.1:p.Val64= | |
| NM_005458.8:c.484G= MANE Select | NP_005449.5:p.Val162= |