Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.48527228A>T , CM000685.2:g.48527228A>T | GRCh38 |
| NC_000023.10:g.48385616A>T , CM000685.1:g.48385616A>T | GRCh37 |
| NC_000023.9:g.48270560A>T | NCBI36 |
| NG_007452.1:g.10453A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000495186.6:c.412A>T MANE Select | ENSP00000417052.1:p.Ile138Phe | |
| ENST00000651615.1:c.412A>T | ENSP00000498524.1:p.Ile138Phe | |
| ENST00000276096.10:n.370A>T | ||
| ENST00000414061.1:c.412A>T | ENSP00000405832.1:p.Ile138Phe | |
| ENST00000446158.5:c.412A>T | ENSP00000390031.1:p.Ile138Phe | |
| ENST00000466461.1:n.251A>T | ||
| ENST00000495186.5:c.412A>T | ENSP00000417052.1:p.Ile138Phe | |
| ENST00000498425.1:n.533A>T | ||
| NM_006579.2:c.412A>T | NP_006570.1:p.Ile138Phe | |
| NM_006579.3:c.412A>T MANE Select | NP_006570.1:p.Ile138Phe |