Linked Data
ClinVar Variation Id:
334757
dbSNP Id:
rs759455097
ExAC:
2:228113206 C / T
gnomAD v2:
2-228113206-C-T
gnomAD v3:
2-227248490-C-T
gnomAD v4:
2-227248490-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.227248490C>T , CM000664.2:g.227248490C>T | GRCh38 |
| NC_000002.11:g.228113206C>T , CM000664.1:g.228113206C>T | GRCh37 |
| NC_000002.10:g.227821450C>T | NCBI36 |
| NG_011591.1:g.88926C>T , LRG_230:g.88926C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000396578.8:c.516C>T (COL4A3) MANE Select | ENSP00000379823.3:p.Asp172= | |
| ENST00000396578.7:c.516C>T (COL4A3) | ENSP00000379823.3:p.Asp172= | |
| NM_000091.4:c.516C>T , LRG_230t1:c.516C>T (COL4A3) | NP_000082.2:p.Asp172= | |
| NR_102371.1:n.1593-10316G>A (MFF-DT) | ||
| XM_005246276.2:c.516C>T (COL4A3) | XP_005246333.1:p.Asp172= | |
| XM_005246277.2:c.516C>T (COL4A3) | XP_005246334.1:p.Asp172= | |
| XM_005246280.2:c.516C>T (COL4A3) | XP_005246337.1:p.Asp172= | |
| XM_006712245.2:c.516C>T (COL4A3) | XP_006712308.1:p.Asp172= | |
| XM_011510555.1:c.516C>T (COL4A3) | XP_011508857.1:p.Asp172= | |
| XR_241280.2:n.654C>T (COL4A3) | ||
| XM_005246277.3:c.516C>T (COL4A3) | XP_005246334.1:p.Asp172= | |
| XM_005246280.3:c.516C>T (COL4A3) | XP_005246337.1:p.Asp172= | |
| XM_006712245.3:c.516C>T (COL4A3) | XP_006712308.1:p.Asp172= | |
| XM_017003295.1:c.516C>T (COL4A3) | XP_016858784.1:p.Asp172= | |
| XR_001738601.1:n.654C>T (COL4A3) | ||
| XR_241280.3:n.654C>T (COL4A3) | ||
| NM_000091.5:c.516C>T (COL4A3) MANE Select | NP_000082.2:p.Asp172= |