Linked Data
ClinVar Variation Id:
297331
ClinVar RCV Id:
RCV000267508
dbSNP Id:
rs1057515528
gnomAD v3:
1-42734550-C-T
gnomAD v4:
1-42734550-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.42734550C>T , CM000663.2:g.42734550C>T | GRCh38 |
| NC_000001.10:g.43200221C>T , CM000663.1:g.43200221C>T | GRCh37 |
| NC_000001.9:g.42972808C>T | NCBI36 |
| NG_008993.1:g.10705G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296387.6:c.*536G>A MANE Select | ENSP00000296387.1:n.*536G>A | |
| ENST00000296387.5:c.*536G>A | ENSP00000296387.1:n.*536G>A | |
| ENST00000539749.5:c.*1212G>A | ENSP00000443229.1:n.*1212G>A | |
| NM_001123395.1:c.*1318G>A | NP_001116867.1:n.*1318G>A | |
| NM_001185117.1:c.*1212G>A | NP_001172046.1:n.*1212G>A | |
| NM_148960.2:c.*536G>A | NP_683763.2:n.*536G>A | |
| NM_001123395.2:c.*1318G>A | NP_001116867.1:n.*1318G>A | |
| NM_148960.3:c.*536G>A MANE Select | NP_683763.2:n.*536G>A | |
| NM_001185117.2:c.*1212G>A | NP_001172046.1:n.*1212G>A |