Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.12887082A>T , CM000681.2:g.12887082A>T | GRCh38 |
| NC_000019.9:g.12997896A>T , CM000681.1:g.12997896A>T | GRCh37 |
| NC_000019.8:g.12858896A>T | NCBI36 |
| NG_009292.1:g.923A>T | |
| NG_013087.1:g.5122T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264834.6:c.59T>A MANE Select | ENSP00000264834.3:p.Phe20Tyr | |
| ENST00000264834.4:c.59T>A | ENSP00000264834.3:p.Phe20Tyr | |
| NM_006563.3:c.59T>A | NP_006554.1:p.Phe20Tyr | |
| XM_011527642.1:c.-145T>A | XP_011525944.1:n.-145T>A | |
| NM_006563.4:c.59T>A | NP_006554.1:p.Phe20Tyr | |
| XM_011527642.2:c.-145T>A | XP_011525944.1:n.-145T>A | |
| NM_006563.5:c.59T>A MANE Select | NP_006554.1:p.Phe20Tyr |