Linked Data
ClinVar Variation Id:
1428943
ClinVar RCV Id:
RCV001967122
dbSNP Id:
rs769581869
ExAC:
20:10639113 T / C
gnomAD v2:
20-10639113-T-C
gnomAD v4:
20-10658465-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10658465T>C , CM000682.2:g.10658465T>C | GRCh38 |
| NC_000020.10:g.10639113T>C , CM000682.1:g.10639113T>C | GRCh37 |
| NC_000020.9:g.10587113T>C | NCBI36 |
| NG_007496.1:g.20582A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000254958.10:c.694+3A>G MANE Select | ENSP00000254958.4:n.694+3A>G | |
| ENST00000254958.9:c.694+3A>G | ENSP00000254958.4:n.694+3A>G | |
| ENST00000423891.6:n.560+3A>G | ||
| NM_000214.2:c.694+3A>G | NP_000205.1:n.694+3A>G | |
| NM_000214.3:c.694+3A>G MANE Select | NP_000205.1:n.694+3A>G |