Linked Data
gnomAD v4:
15-80591694-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.80591694A>C , CM000677.2:g.80591694A>C | GRCh38 |
| NC_000015.9:g.80884035A>C , CM000677.1:g.80884035A>C | GRCh37 |
| NC_000015.8:g.78671090A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000303329.9:c.2045A>C MANE Select | ENSP00000307479.4:p.Glu682Ala | |
| ENST00000303329.8:c.2045A>C | ENSP00000307479.4:p.Glu682Ala | |
| ENST00000527771.5:c.2012A>C | ENSP00000453792.1:p.Glu671Ala | |
| ENST00000533983.5:c.2012A>C | ENSP00000453651.1:p.Glu671Ala | |
| ENST00000610490.4:c.*343A>C | ENSP00000483762.1:n.*343A>C | |
| ENST00000622346.4:c.2045A>C | ENSP00000479393.1:p.Glu682Ala | |
| NM_014862.3:c.2045A>C | NP_055677.3:p.Glu682Ala | |
| NM_014862.4:c.2045A>C MANE Select | NP_055677.3:p.Glu682Ala |