Linked Data
ClinVar Variation Id:
1113861
ClinVar RCV Id:
RCV001441397
dbSNP Id:
rs1847546876
gnomAD v4:
11-5226437-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5226437T>C , CM000673.2:g.5226437T>C | GRCh38 |
| NC_000011.9:g.5247667T>C , CM000673.1:g.5247667T>C | GRCh37 |
| NC_000011.8:g.5204243T>C | NCBI36 |
| NG_000007.3:g.71179A>G | |
| NG_059281.1:g.5635A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647020.1:c.315+140A>G | ENSP00000494175.1:n.315+140A>G | |
| ENST00000335295.4:c.315+140A>G MANE Select | ENSP00000333994.3:n.315+140A>G | |
| ENST00000475226.1:n.247+140A>G | ||
| ENST00000485743.1:n.506A>G | ||
| ENST00000633227.1:c.*131+140A>G | ENSP00000488004.1:n.*131+140A>G | |
| NM_000518.4:c.315+140A>G | NP_000509.1:n.315+140A>G | |
| NM_000518.5:c.315+140A>G MANE Select | NP_000509.1:n.315+140A>G |