Linked Data
ClinVar Variation Id:
1284647
ClinVar RCV Id:
RCV001699858
dbSNP Id:
rs373088068
ExAC:
8:19809316 G / C
gnomAD v2:
8-19809316-G-C
gnomAD v3:
8-19951805-G-C
gnomAD v4:
8-19951805-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.19951805G>C , CM000670.2:g.19951805G>C | GRCh38 |
| NC_000008.10:g.19809316G>C , CM000670.1:g.19809316G>C | GRCh37 |
| NC_000008.9:g.19853596G>C | NCBI36 |
| NG_008855.1:g.17735G>C | |
| NG_008855.2:g.55089G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650287.1:c.286G>C MANE Select | ENSP00000497642.1:p.Val96Leu | |
| ENST00000311322.8:c.286G>C | ENSP00000309757.6:p.Val96Leu | |
| ENST00000520959.5:c.58G>C | ENSP00000428496.1:p.Val20Leu | |
| ENST00000521994.1:n.543G>C | ||
| ENST00000522701.5:c.286G>C | ENSP00000428557.1:p.Val96Leu | |
| ENST00000524029.5:c.286G>C | ENSP00000428237.1:p.Val96Leu | |
| NM_000237.2:c.286G>C | NP_000228.1:p.Val96Leu | |
| NM_000237.3:c.286G>C MANE Select | NP_000228.1:p.Val96Leu |