Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.88719704A>T , CM000678.2:g.88719704A>T | GRCh38 |
| NC_000016.9:g.88786112A>T , CM000678.1:g.88786112A>T | GRCh37 |
| NC_000016.8:g.87313613A>T | NCBI36 |
| NG_042229.1:g.70517T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301015.14:c.6341T>A MANE Select | ENSP00000301015.9:p.Phe2114Tyr | |
| ENST00000466823.3:c.367T>A | ||
| ENST00000301015.13:c.6341T>A | ENSP00000301015.9:p.Phe2114Tyr | |
| ENST00000419505.5:c.107T>A | ENSP00000406358.1:p.Phe36Tyr | |
| ENST00000466823.2:c.367T>A | ||
| ENST00000495568.7:n.582T>A | ||
| ENST00000497793.2:n.496T>A | ||
| NM_001142864.2:c.6341T>A | NP_001136336.2:p.Phe2114Tyr | |
| NM_001142864.3:c.6341T>A | NP_001136336.2:p.Phe2114Tyr | |
| NM_001142864.4:c.6341T>A MANE Select | NP_001136336.2:p.Phe2114Tyr |