Linked Data
ClinVar Variation Id:
1763947
ClinVar RCV Id:
RCV002447926
dbSNP Id:
rs1369185858
gnomAD v2:
10-48414010-C-T
gnomAD v3:
10-47325352-G-A
gnomAD v4:
10-47325352-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.47325352G>A , CM000672.2:g.47325352G>A | GRCh38 |
| NC_000010.10:g.48414010C>T , CM000672.1:g.48414010C>T | GRCh37 |
| NC_000010.9:g.48034016C>T | NCBI36 |
| NG_033916.1:g.7863G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000581492.3:c.858G>A MANE Select | ENSP00000463051.1:p.Lys286= | |
| ENST00000581492.2:c.858G>A | ENSP00000463051.1:p.Lys286= | |
| NM_016204.2:c.858G>A | NP_057288.1:p.Lys286= | |
| XM_006717761.2:c.858G>A | XP_006717824.1:p.Lys286= | |
| NM_016204.3:c.858G>A | NP_057288.1:p.Lys286= | |
| NM_016204.4:c.858G>A MANE Select | NP_057288.1:p.Lys286= |