Linked Data
ClinVar Variation Id:
784764
ClinVar RCV Id:
RCV000966535
dbSNP Id:
rs144594313
ExAC:
1:156837971 C / T
gnomAD v2:
1-156837971-C-T
gnomAD v3:
1-156868179-C-T
gnomAD v4:
1-156868179-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.156868179C>T , CM000663.2:g.156868179C>T | GRCh38 |
| NC_000001.10:g.156837971C>T , CM000663.1:g.156837971C>T | GRCh37 |
| NC_000001.9:g.155104595C>T | NCBI36 |
| NG_007493.1:g.57430C>T , LRG_261:g.57430C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000674537.2:c.342C>T | ENSP00000502725.1:p.Gly114= | |
| ENST00000392302.7:c.342C>T | ENSP00000376120.3:p.Gly114= | |
| ENST00000497019.7:c.342C>T | ENSP00000436804.2:p.Gly114= | |
| ENST00000524377.7:c.504C>T MANE Select | ENSP00000431418.1:p.Gly168= | |
| ENST00000674537.1:c.342C>T | ENSP00000502725.1:p.Gly114= | |
| ENST00000358660.3:c.504C>T | ENSP00000351486.3:p.Gly168= | |
| ENST00000368196.7:c.504C>T | ENSP00000357179.3:p.Gly168= | |
| ENST00000392302.6:c.414C>T | ENSP00000376120.2:p.Gly138= | |
| ENST00000489021.6:n.313-5454C>T | ||
| ENST00000497019.6:c.414C>T | ENSP00000436804.1:p.Gly138= | |
| ENST00000524377.5:c.504C>T | ENSP00000431418.1:p.Gly168= | |
| ENST00000530298.5:n.562C>T | ||
| NM_001007792.1:c.414C>T , LRG_261t1:c.414C>T | NP_001007793.1:p.Gly138= | |
| NM_001012331.1:c.504C>T , LRG_261t2:c.504C>T | NP_001012331.1:p.Gly168= | |
| NM_002529.3:c.504C>T , LRG_261t3:c.504C>T | NP_002520.2:p.Gly168= | |
| NM_001012331.2:c.504C>T | NP_001012331.1:p.Gly168= | |
| NM_002529.4:c.504C>T MANE Select | NP_002520.2:p.Gly168= |