Linked Data
ClinVar Variation Id:
1997611
ClinVar RCV Id:
RCV002791861
dbSNP Id:
rs369168168
gnomAD v4:
11-5226898-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5226898C>T , CM000673.2:g.5226898C>T | GRCh38 |
| NC_000011.9:g.5248128C>T , CM000673.1:g.5248128C>T | GRCh37 |
| NC_000011.8:g.5204704C>T | NCBI36 |
| NG_000007.3:g.70718G>A | |
| NG_059281.1:g.5174G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000647020.1:c.92+32G>A | ENSP00000494175.1:n.92+32G>A | |
| ENST00000335295.4:c.92+32G>A MANE Select | ENSP00000333994.3:n.92+32G>A | |
| ENST00000380315.2:c.92+32G>A | ENSP00000369671.2:n.92+32G>A | |
| ENST00000485743.1:n.143+32G>A | ||
| ENST00000633227.1:c.76+48G>A | ENSP00000488004.1:n.76+48G>A | |
| NM_000518.4:c.92+32G>A | NP_000509.1:n.92+32G>A | |
| NM_000518.5:c.92+32G>A MANE Select | NP_000509.1:n.92+32G>A |