Linked Data
ClinVar Variation Id:
666957
dbSNP Id:
rs200192011
ExAC:
4:6304053 C / T
gnomAD v2:
4-6304053-C-T
gnomAD v3:
4-6302326-C-T
gnomAD v4:
4-6302326-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.6302326C>T , CM000666.2:g.6302326C>T | GRCh38 |
| NC_000004.11:g.6304053C>T , CM000666.1:g.6304053C>T | GRCh37 |
| NC_000004.10:g.6354954C>T | NCBI36 |
| NG_011700.1:g.37477C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682275.1:c.2567C>T | ENSP00000507852.1:p.Ala856Val | |
| ENST00000683395.1:c.2508C>T | ||
| ENST00000684087.1:c.2531C>T | ENSP00000506978.1:p.Ala844Val | |
| ENST00000506362.2:c.2282C>T | ENSP00000424103.2:p.Ala761Val | |
| ENST00000673991.1:c.2567C>T | ENSP00000501033.1:p.Ala856Val | |
| ENST00000226760.5:c.2531C>T MANE Select | ENSP00000226760.1:p.Ala844Val | |
| ENST00000503569.5:c.2531C>T | ENSP00000423337.1:p.Ala844Val | |
| ENST00000507765.1:n.2716C>T | ||
| NM_001145853.1:c.2531C>T | NP_001139325.1:p.Ala844Val | |
| NM_006005.3:c.2531C>T MANE Select | NP_005996.2:p.Ala844Val | |
| XM_017008586.1:c.2540C>T | XP_016864075.1:p.Ala847Val |