Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.98542010C>A , CM000671.2:g.98542010C>A | GRCh38 |
| NC_000009.11:g.101304292C>A , CM000671.1:g.101304292C>A | GRCh37 |
| NC_000009.10:g.100344113C>A | NCBI36 |
| NG_016426.1:g.172188G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000259455.4:c.493G>T MANE Select | ENSP00000259455.2:p.Asp165Tyr | |
| ENST00000637410.1:n.271G>T | ||
| ENST00000637717.1:c.109G>T | ENSP00000490789.1:p.Asp37Tyr | |
| ENST00000259455.3:c.493G>T | ENSP00000259455.2:p.Asp165Tyr | |
| ENST00000477471.1:n.280G>T | ||
| ENST00000634227.1:n.267G>T | ||
| NM_005458.7:c.493G>T | NP_005449.5:p.Asp165Tyr | |
| XM_017015331.2:c.199G>T | XP_016870820.1:p.Asp67Tyr | |
| NM_005458.8:c.493G>T MANE Select | NP_005449.5:p.Asp165Tyr |