Linked Data
ClinVar Variation Id:
309195
dbSNP Id:
rs547570693
gnomAD v2:
12-5025019-G-A
gnomAD v3:
12-4915853-G-A
gnomAD v4:
12-4915853-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.4915853G>A , CM000674.2:g.4915853G>A | GRCh38 |
| NC_000012.11:g.5025019G>A , CM000674.1:g.5025019G>A | GRCh37 |
| NC_000012.10:g.4895280G>A | NCBI36 |
| NG_011815.1:g.10947G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382545.5:c.*2987G>A MANE Select | ENSP00000371985.3:n.*2987G>A | |
| ENST00000543874.3:n.106-1933G>A | ||
| ENST00000639306.1:c.2184-1933G>A | ENSP00000492506.1:n.2184-1933G>A | |
| ENST00000639680.1:c.160-1933G>A | ||
| ENST00000382545.3:c.*2987G>A | ENSP00000371985.3:n.*2987G>A | |
| ENST00000541095.1:n.105+5381G>A | ||
| ENST00000543874.2:n.97-1933G>A | ||
| NM_000217.2:c.*2987G>A | NP_000208.2:n.*2987G>A | |
| NM_000217.3:c.*2987G>A MANE Select | NP_000208.2:n.*2987G>A |