Linked Data
ClinVar Variation Id:
566746
ClinVar RCV Id:
RCV000686638
dbSNP Id:
rs765166524
ExAC:
12:5155145 C / A
gnomAD v2:
12-5155145-C-A
gnomAD v4:
12-5045979-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.5045979C>A , CM000674.2:g.5045979C>A | GRCh38 |
| NC_000012.11:g.5155145C>A , CM000674.1:g.5155145C>A | GRCh37 |
| NC_000012.10:g.5025406C>A | NCBI36 |
| NG_012198.1:g.7061C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252321.5:c.1832C>A MANE Select | ENSP00000252321.3:p.Thr611Lys | |
| ENST00000252321.4:c.1832C>A | ENSP00000252321.3:p.Thr611Lys | |
| NM_002234.3:c.1832C>A | NP_002225.2:p.Thr611Lys | |
| NM_002234.4:c.1832C>A MANE Select | NP_002225.2:p.Thr611Lys |