Linked Data
ClinVar Variation Id:
1565483
ClinVar RCV Id:
RCV002218337
dbSNP Id:
rs769080198
ExAC:
19:6697445 C / T
gnomAD v2:
19-6697445-C-T
gnomAD v3:
19-6697434-C-T
gnomAD v4:
19-6697434-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.6697434C>T , CM000681.2:g.6697434C>T | GRCh38 |
| NC_000019.9:g.6697445C>T , CM000681.1:g.6697445C>T | GRCh37 |
| NC_000019.8:g.6648445C>T | NCBI36 |
| NG_009557.1:g.28218G>A , LRG_27:g.28218G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695651.1:n.1054G>A | ||
| ENST00000695652.1:c.2583G>A | ENSP00000512083.1:p.Pro861= | |
| ENST00000695653.1:c.615G>A | ENSP00000512084.1:p.Pro205= | |
| ENST00000695654.1:c.1830G>A | ENSP00000512085.1:p.Pro610= | |
| ENST00000695655.1:c.1647G>A | ENSP00000512086.1:n.1647G>A | |
| ENST00000695692.1:n.2070G>A | ||
| ENST00000245907.11:c.2706G>A MANE Select | ENSP00000245907.4:p.Pro902= | |
| ENST00000245907.10:c.2706G>A | ENSP00000245907.4:p.Pro902= | |
| ENST00000594005.1:n.282G>A | ||
| NM_000064.3:c.2706G>A | NP_000055.2:p.Pro902= | |
| NM_000064.4:c.2706G>A MANE Select | NP_000055.2:p.Pro902= |