Linked Data
gnomAD v4:
1-216247202-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.216247202A>T , CM000663.2:g.216247202A>T | GRCh38 |
| NC_000001.10:g.216420544A>T , CM000663.1:g.216420544A>T | GRCh37 |
| NC_000001.9:g.214487167A>T | NCBI36 |
| NG_009497.1:g.181195T>A | |
| NG_009497.2:g.181247T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307340.8:c.2192T>A MANE Select | ENSP00000305941.3:p.Phe731Tyr | |
| ENST00000674083.1:c.2192T>A | ENSP00000501296.1:p.Phe731Tyr | |
| ENST00000307340.7:c.2192T>A | ENSP00000305941.3:p.Phe731Tyr | |
| ENST00000366942.3:c.2192T>A | ENSP00000355909.3:p.Phe731Tyr | |
| NM_007123.5:c.2192T>A | NP_009054.5:p.Phe731Tyr | |
| NM_206933.2:c.2192T>A | NP_996816.2:p.Phe731Tyr | |
| NM_206933.3:c.2192T>A | NP_996816.2:p.Phe731Tyr | |
| NM_007123.6:c.2192T>A | NP_009054.6:p.Phe731Tyr | |
| NM_206933.4:c.2192T>A MANE Select | NP_996816.3:p.Phe731Tyr |