Linked Data
ClinVar Variation Id:
1315619
dbSNP Id:
rs373587423
ExAC:
16:14029282 T / C
gnomAD v2:
16-14029282-T-C
gnomAD v3:
16-13935425-T-C
gnomAD v4:
16-13935425-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.13935425T>C , CM000678.2:g.13935425T>C | GRCh38 |
| NC_000016.9:g.14029282T>C , CM000678.1:g.14029282T>C | GRCh37 |
| NC_000016.8:g.13936783T>C | NCBI36 |
| NG_011442.1:g.20269T>C , LRG_463:g.20269T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682568.1:n.1571T>C | ||
| ENST00000682617.1:c.1631T>C | ENSP00000507912.1:p.Val544Ala | |
| ENST00000682826.1:c.*807T>C | ENSP00000507274.1:n.*807T>C | |
| ENST00000682909.1:n.3533T>C | ||
| ENST00000683277.1:n.3138T>C | ||
| ENST00000683407.1:n.1501T>C | ||
| ENST00000683962.1:c.*1187T>C | ENSP00000506854.1:n.*1187T>C | |
| ENST00000311895.8:c.1493T>C MANE Select | ENSP00000310520.7:p.Val498Ala | |
| ENST00000311895.7:c.1493T>C | ENSP00000310520.7:p.Val498Ala | |
| ENST00000389138.7:n.770T>C | ||
| NM_005236.2:c.1493T>C , LRG_463t1:c.1493T>C | NP_005227.1:p.Val498Ala | |
| XM_011522424.1:c.1631T>C | XP_011520726.1:p.Val544Ala | |
| XM_011522425.1:c.950T>C | XP_011520727.1:p.Val317Ala | |
| XM_011522426.1:c.704T>C | XP_011520728.1:p.Val235Ala | |
| XM_011522427.1:c.143T>C | XP_011520729.1:p.Val48Ala | |
| XR_932805.1:n.1652T>C | ||
| XM_011522424.3:c.1631T>C | XP_011520726.1:p.Val544Ala | |
| XM_017023043.2:c.704T>C | XP_016878532.1:p.Val235Ala | |
| NM_005236.3:c.1493T>C MANE Select | NP_005227.1:p.Val498Ala |