Linked Data
ClinVar Variation Id:
229619
dbSNP Id:
rs138607917
ExAC:
1:215848430 A / T
gnomAD v2:
1-215848430-A-T
gnomAD v3:
1-215675088-A-T
gnomAD v4:
1-215675088-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.215675088A>T , CM000663.2:g.215675088A>T | GRCh38 |
| NC_000001.10:g.215848430A>T , CM000663.1:g.215848430A>T | GRCh37 |
| NC_000001.9:g.213915053A>T | NCBI36 |
| NG_009497.1:g.753309T>A | |
| NG_009497.2:g.753361T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307340.8:c.12823T>A MANE Select | ENSP00000305941.3:p.Ser4275Thr | |
| ENST00000674083.1:c.12823T>A | ENSP00000501296.1:p.Ser4275Thr | |
| ENST00000307340.7:c.12823T>A | ENSP00000305941.3:p.Ser4275Thr | |
| NM_206933.2:c.12823T>A | NP_996816.2:p.Ser4275Thr | |
| NM_206933.3:c.12823T>A | NP_996816.2:p.Ser4275Thr | |
| NM_206933.4:c.12823T>A MANE Select | NP_996816.3:p.Ser4275Thr |