Linked Data
ClinVar Variation Id:
203226
dbSNP Id:
rs565638291
ExAC:
2:179605556 T / C
gnomAD v2:
2-179605556-T-C
gnomAD v3:
2-178740829-T-C
gnomAD v4:
2-178740829-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.178740829T>C , CM000664.2:g.178740829T>C | GRCh38 |
| NC_000002.11:g.179605556T>C , CM000664.1:g.179605556T>C | GRCh37 |
| NC_000002.10:g.179313801T>C | NCBI36 |
| NG_011618.3:g.94974A>G , LRG_391:g.94974A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342992.11:c.10361-2469A>G | ENSP00000343764.6:n.10361-2469A>G | |
| ENST00000342175.11:c.11891A>G | ENSP00000340554.6:p.Asn3964Ser | |
| ENST00000359218.10:c.11690A>G | ENSP00000352154.5:p.Asn3897Ser | |
| ENST00000342175.10:c.11891A>G | ENSP00000340554.6:p.Asn3964Ser | |
| ENST00000342992.10:c.10361-2469A>G | ENSP00000343764.6:n.10361-2469A>G | |
| ENST00000359218.9:c.11690A>G | ENSP00000352154.5:p.Asn3897Ser | |
| ENST00000460472.6:c.11315A>G | ENSP00000434586.1:p.Asn3772Ser | |
| ENST00000589042.5:c.12404A>G MANE Select | ENSP00000467141.1:p.Asn4135Ser | |
| ENST00000591111.5:c.11453A>G | ENSP00000465570.1:p.Asn3818Ser | |
| ENST00000615779.4:c.11453A>G | ENSP00000483597.1:p.Asn3818Ser | |
| NM_001256850.1:c.11453A>G | NP_001243779.1:p.Asn3818Ser | |
| NM_001267550.2:c.12404A>G MANE Select | NP_001254479.2:p.Asn4135Ser | |
| NM_003319.4:c.11315A>G | NP_003310.4:p.Asn3772Ser | |
| NM_133378.4:c.10361-2469A>G | NP_596869.4:n.10361-2469A>G | |
| NM_133432.3:c.11690A>G | NP_597676.3:p.Asn3897Ser | |
| NM_133437.4:c.11891A>G | NP_597681.4:p.Asn3964Ser | |
| XM_011511729.1:c.11501A>G | XP_011510031.1:p.Asn3834Ser | |
| XM_011511730.1:c.11501A>G | XP_011510032.1:p.Asn3834Ser | |
| XM_011511731.1:c.11360A>G | XP_011510033.1:p.Asn3787Ser | |
| XM_017004819.1:c.11456A>G | XP_016860308.1:p.Asn3819Ser | |
| XM_017004820.1:c.10364-2469A>G | XP_016860309.1:n.10364-2469A>G | |
| XM_017004821.1:c.10361-2469A>G | XP_016860310.1:n.10361-2469A>G | |
| XM_017004822.1:c.11456A>G | XP_016860311.1:p.Asn3819Ser | |
| XM_017004823.1:c.11456A>G | XP_016860312.1:p.Asn3819Ser | |
| XM_024453094.1:c.11456A>G | XP_024308862.1:p.Asn3819Ser | |
| XM_024453095.1:c.11456A>G | XP_024308863.1:p.Asn3819Ser | |
| XM_024453096.1:c.11456A>G | XP_024308864.1:p.Asn3819Ser | |
| XM_024453097.1:c.11456A>G | XP_024308865.1:p.Asn3819Ser | |
| XM_024453098.1:c.11456A>G | XP_024308866.1:p.Asn3819Ser | |
| XM_024453099.1:c.11456A>G | XP_024308867.1:p.Asn3819Ser |