Linked Data
ClinVar Variation Id:
1526032
ClinVar RCV Id:
RCV002052052
dbSNP Id:
rs1555132614
gnomAD v2:
12-6979491-G-A
gnomAD v4:
12-6870327-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.6870327G>A , CM000674.2:g.6870327G>A | GRCh38 |
| NC_000012.11:g.6979491G>A , CM000674.1:g.6979491G>A | GRCh37 |
| NC_000012.10:g.6849752G>A | NCBI36 |
| NG_011948.1:g.7908G>A | |
| NG_013308.1:g.8031C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000396705.10:c.694G>A MANE Select | ENSP00000379933.4:p.Val232Met | |
| ENST00000229270.8:c.805G>A | ENSP00000229270.4:p.Val269Met | |
| ENST00000396705.9:c.694G>A | ENSP00000379933.4:p.Val232Met | |
| ENST00000474253.1:n.183G>A | ||
| ENST00000488464.6:c.448G>A | ENSP00000475620.1:p.Val150Met | |
| ENST00000535434.5:c.448G>A | ENSP00000443599.1:p.Val150Met | |
| ENST00000613953.4:c.805G>A | ENSP00000484435.1:p.Val269Met | |
| NM_000365.5:c.694G>A | NP_000356.1:p.Val232Met | |
| NM_001159287.1:c.805G>A | NP_001152759.1:p.Val269Met | |
| NM_001258026.1:c.448G>A | NP_001244955.1:p.Val150Met | |
| XR_002957378.1:n.1702G>A | ||
| NM_000365.6:c.694G>A MANE Select | NP_000356.1:p.Val232Met | |
| NM_001258026.2:c.448G>A | NP_001244955.1:p.Val150Met |