Linked Data
ClinVar Variation Id:
306365
ClinVar RCV Id:
RCV000270259
dbSNP Id:
rs10898563
gnomAD v2:
11-86659213-A-G
gnomAD v3:
11-86948171-A-G
gnomAD v4:
11-86948171-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.86948171A>G , CM000673.2:g.86948171A>G | GRCh38 |
| NC_000011.9:g.86659213A>G , CM000673.1:g.86659213A>G | GRCh37 |
| NC_000011.8:g.86336861A>G | NCBI36 |
| NG_011752.1:g.12221T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000531380.2:c.*2971T>C (FZD4) MANE Select | ENSP00000434034.1:n.*2971T>C | |
| ENST00000528769.5:n.129-2185A>G (PRSS23) | ||
| ENST00000531380.1:c.*2971T>C (FZD4) | ENSP00000434034.1:n.*2971T>C | |
| ENST00000531521.1:n.243-2185A>G (PRSS23) | ||
| ENST00000532234.5:c.*65-2185A>G (PRSS23) | ENSP00000436676.1:n.*65-2185A>G | |
| ENST00000533902.2:c.207-3045A>G (PRSS23) | ENSP00000437268.1:n.207-3045A>G | |
| NM_012193.3:c.*2971T>C (FZD4) | NP_036325.2:n.*2971T>C | |
| NR_120591.1:n.737-2185A>G (PRSS23) | ||
| NR_120592.1:n.630-3045A>G (PRSS23) | ||
| NR_120591.2:n.435-2185A>G (PRSS23) | ||
| NR_120592.2:n.328-3045A>G (PRSS23) | ||
| NM_012193.4:c.*2971T>C (FZD4) MANE Select | NP_036325.2:n.*2971T>C | |
| NR_120591.3:n.435-2185A>G (PRSS23) |