Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.98541940T>A , CM000671.2:g.98541940T>A | GRCh38 |
| NC_000009.11:g.101304222T>A , CM000671.1:g.101304222T>A | GRCh37 |
| NC_000009.10:g.100344043T>A | NCBI36 |
| NG_016426.1:g.172258A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000259455.4:c.563A>T MANE Select | ENSP00000259455.2:p.Lys188Met | |
| ENST00000637410.1:n.341A>T | ||
| ENST00000637717.1:c.179A>T | ENSP00000490789.1:p.Lys60Met | |
| ENST00000259455.3:c.563A>T | ENSP00000259455.2:p.Lys188Met | |
| ENST00000477471.1:n.350A>T | ||
| ENST00000634227.1:n.337A>T | ||
| NM_005458.7:c.563A>T | NP_005449.5:p.Lys188Met | |
| XM_017015331.2:c.269A>T | XP_016870820.1:p.Lys90Met | |
| NM_005458.8:c.563A>T MANE Select | NP_005449.5:p.Lys188Met |