Linked Data
ClinVar Variation Id:
939430
ClinVar RCV Id:
RCV001208833
dbSNP Id:
rs142063347
gnomAD v2:
22-50658896-G-A
gnomAD v3:
22-50220467-G-A
gnomAD v4:
22-50220467-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.50220467G>A , CM000684.2:g.50220467G>A | GRCh38 |
| NC_000022.10:g.50658896G>A , CM000684.1:g.50658896G>A | GRCh37 |
| NC_000022.9:g.49001023G>A | NCBI36 |
| NG_032160.1:g.29505C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000248846.10:c.3892C>T MANE Select | ENSP00000248846.5:p.Pro1298Ser | |
| ENST00000248846.9:c.3892C>T | ENSP00000248846.5:p.Pro1298Ser | |
| ENST00000439308.6:c.3892C>T | ENSP00000397387.2:p.Pro1298Ser | |
| ENST00000491449.5:n.2199C>T | ||
| ENST00000498611.5:n.3618-452C>T | ||
| NM_020461.3:c.3892C>T | NP_065194.2:p.Pro1298Ser | |
| XR_938347.1:n.4457C>T | ||
| XR_938348.1:n.3050-452C>T | ||
| XR_001755343.2:n.4461C>T | ||
| XR_001755344.2:n.4461C>T | ||
| XR_002958720.1:n.3054-452C>T | ||
| XR_938347.2:n.4461C>T | ||
| NM_020461.4:c.3892C>T MANE Select | NP_065194.3:p.Pro1298Ser |