Linked Data
ClinVar Variation Id:
1692907
ClinVar RCV Id:
RCV002259281
dbSNP Id:
rs878854800
MyVariant Identifiers:
chr5:g.131911606C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.132575914C>A , CM000667.2:g.132575914C>A | GRCh38 |
| NC_000005.9:g.131911606C>A , CM000667.1:g.131911606C>A | GRCh37 |
| NC_000005.8:g.131939505C>A | NCBI36 |
| NG_021151.1:g.23991C>A | |
| NG_021151.2:g.23938C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378823.8:c.351C>A MANE Select | ENSP00000368100.4:p.Val117= | |
| ENST00000638452.2:c.54C>A | ENSP00000492349.2:p.Val18= | |
| ENST00000638504.1:n.428C>A | ||
| ENST00000638568.2:c.54C>A | ENSP00000491158.2:p.Val18= | |
| ENST00000639899.1:n.511C>A | ||
| ENST00000640655.2:c.54C>A | ENSP00000491596.2:p.Val18= | |
| ENST00000651160.1:c.351C>A | ENSP00000498829.1:p.Val117= | |
| ENST00000651541.1:c.54C>A | ENSP00000498795.1:p.Val18= | |
| ENST00000651658.1:n.419C>A | ||
| ENST00000651723.1:c.*448+51C>A | ENSP00000498237.1:n.*448+51C>A | |
| ENST00000652016.1:c.351C>A | ENSP00000498267.1:p.Val117= | |
| ENST00000652485.1:c.351C>A | ENSP00000498973.1:p.Val117= | |
| ENST00000378823.7:c.351C>A | ENSP00000368100.4:p.Val117= | |
| ENST00000416135.5:c.54C>A | ENSP00000389515.1:p.Val18= | |
| ENST00000423956.5:c.351C>A | ENSP00000390971.1:p.Val117= | |
| ENST00000453394.5:c.351C>A | ENSP00000400049.1:p.Val117= | |
| ENST00000533482.5:c.300+51C>A | ENSP00000431225.1:n.300+51C>A | |
| NM_005732.3:c.351C>A | NP_005723.2:p.Val117= | |
| NM_005732.4:c.351C>A MANE Select | NP_005723.2:p.Val117= |