Linked Data
ClinVar Variation Id:
2698386
ClinVar RCV Id:
RCV003551728
MyVariant Identifiers:
chr3:g.183853215T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.184135427T>C , CM000665.2:g.184135427T>C | GRCh38 |
| NC_000003.11:g.183853215T>C , CM000665.1:g.183853215T>C | GRCh37 |
| NC_000003.10:g.185335909T>C | NCBI36 |
| NG_015826.1:g.5406T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000432569.2:c.42T>C | ENSP00000414775.1:p.Ser14= | |
| ENST00000465218.3:n.65T>C | ||
| ENST00000468748.7:n.25T>C | ||
| ENST00000471832.2:c.42T>C | ENSP00000497786.1:p.Ser14= | |
| ENST00000492226.2:n.39T>C | ||
| ENST00000647636.1:c.42T>C | ENSP00000497505.1:p.Ser14= | |
| ENST00000647909.1:c.42T>C | ENSP00000498164.1:p.Ser14= | |
| ENST00000648314.1:c.42T>C | ENSP00000496920.1:p.Ser14= | |
| ENST00000648599.1:c.42T>C | ENSP00000497159.1:p.Ser14= | |
| ENST00000648630.1:c.36T>C | ENSP00000497887.1:p.Ser12= | |
| ENST00000648682.1:c.42T>C | ENSP00000498185.1:p.Ser14= | |
| ENST00000648882.1:c.42T>C | ENSP00000497603.1:p.Ser14= | |
| ENST00000648890.1:c.42T>C | ENSP00000497503.1:p.Ser14= | |
| ENST00000648915.2:c.42T>C MANE Select | ENSP00000497160.1:p.Ser14= | |
| ENST00000649688.1:c.42T>C | ENSP00000497097.1:p.Ser14= | |
| ENST00000649814.1:n.91T>C | ||
| ENST00000273783.7:c.42T>C | ENSP00000273783.3:p.Ser14= | |
| ENST00000432569.1:c.42T>C | ENSP00000414775.1:p.Ser14= | |
| ENST00000432982.5:c.28T>C | ||
| ENST00000444495.1:c.42T>C | ENSP00000409142.1:p.Ser14= | |
| ENST00000481054.5:n.43T>C | ||
| ENST00000491144.5:n.390T>C | ||
| NM_003907.2:c.42T>C | NP_003898.2:p.Ser14= | |
| XR_924208.1:n.993T>C | ||
| NM_003907.3:c.42T>C MANE Select | NP_003898.2:p.Ser14= | |
| XM_011513266.3:c.-860T>C | XP_011511568.1:n.-860T>C | |
| XR_001740352.2:n.405T>C | ||
| XR_001740353.2:n.405T>C | ||
| XR_924208.2:n.405T>C |