Linked Data
gnomAD v4:
11-118312807-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.118312807G>A , CM000673.2:g.118312807G>A | GRCh38 |
| NC_000011.9:g.118183522G>A , CM000673.1:g.118183522G>A | GRCh37 |
| NC_000011.8:g.117688732G>A | NCBI36 |
| NG_007383.1:g.13228G>A , LRG_38:g.13228G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361763.9:c.293G>A MANE Select | ENSP00000354566.4:p.Cys98Tyr | |
| ENST00000361763.8:c.293G>A | ENSP00000354566.4:p.Cys98Tyr | |
| ENST00000526146.5:n.839G>A | ||
| ENST00000528435.5:n.846G>A | ||
| ENST00000528600.1:c.275G>A | ENSP00000433975.1:p.Cys92Tyr | |
| ENST00000529713.5:n.399G>A | ||
| ENST00000531913.1:n.664G>A | ||
| NM_000733.3:c.293G>A , LRG_38t1:c.293G>A | NP_000724.1:p.Cys98Tyr | |
| NM_000733.4:c.293G>A MANE Select | NP_000724.1:p.Cys98Tyr |