Linked Data
ClinVar Variation Id:
334786
dbSNP Id:
rs200512461
ExAC:
2:228173675 A / G
gnomAD v2:
2-228173675-A-G
gnomAD v3:
2-227308959-A-G
gnomAD v4:
2-227308959-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.227308959A>G , CM000664.2:g.227308959A>G | GRCh38 |
| NC_000002.11:g.228173675A>G , CM000664.1:g.228173675A>G | GRCh37 |
| NC_000002.10:g.227881919A>G | NCBI36 |
| NG_011591.1:g.149395A>G , LRG_230:g.149395A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000471862.2:n.1781A>G (COL4A3) | ||
| ENST00000683077.1:n.5A>G (COL4A3) | ||
| ENST00000684413.1:n.1963A>G (COL4A3) | ||
| ENST00000396578.8:c.4523A>G (COL4A3) MANE Select | ENSP00000379823.3:p.Asn1508Ser | |
| ENST00000469504.2:c.434-245A>G (COL4A3) | ENSP00000493493.1:n.434-245A>G | |
| ENST00000643388.1:c.209A>G (COL4A3) | ENSP00000495177.1:p.Asn70Ser | |
| ENST00000396578.7:c.4523A>G (COL4A3) | ENSP00000379823.3:p.Asn1508Ser | |
| ENST00000469504.1:n.149-245A>G (COL4A3) | ||
| NM_000091.4:c.4523A>G , LRG_230t1:c.4523A>G (COL4A3) | NP_000082.2:p.Asn1508Ser | |
| NR_102371.1:n.48-3304T>C (MFF-DT) | ||
| XM_005246276.2:c.4523A>G (COL4A3) | XP_005246333.1:p.Asn1508Ser | |
| XM_005246277.2:c.4418A>G (COL4A3) | XP_005246334.1:p.Asn1473Ser | |
| XM_011510555.1:c.4523A>G (COL4A3) | XP_011508857.1:p.Asn1508Ser | |
| XM_011510556.1:c.3284A>G (COL4A3) | XP_011508858.1:p.Asn1095Ser | |
| XR_241280.2:n.4601-245A>G (COL4A3) | ||
| XM_005246277.3:c.4418A>G (COL4A3) | XP_005246334.1:p.Asn1473Ser | |
| XM_011510556.2:c.3284A>G (COL4A3) | XP_011508858.1:p.Asn1095Ser | |
| XR_241280.3:n.4601-245A>G (COL4A3) | ||
| NM_000091.5:c.4523A>G (COL4A3) MANE Select | NP_000082.2:p.Asn1508Ser |