Linked Data
ClinVar Variation Id:
181511
ClinVar RCV Id:
RCV000159083
dbSNP Id:
rs201553362
ExAC:
3:12632424 C / T
gnomAD v2:
3-12632424-C-T
gnomAD v3:
3-12590925-C-T
gnomAD v4:
3-12590925-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.12590925C>T , CM000665.2:g.12590925C>T | GRCh38 |
| NC_000003.11:g.12632424C>T , CM000665.1:g.12632424C>T | GRCh37 |
| NC_000003.10:g.12607424C>T | NCBI36 |
| NG_007467.1:g.78255G>A , LRG_413:g.78255G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000423275.6:c.*908G>A | ENSP00000401088.1:n.*908G>A | |
| ENST00000432427.3:c.560G>A | ||
| ENST00000460610.2:n.37G>A | ||
| ENST00000465826.6:n.834G>A | ||
| ENST00000475353.2:n.1165G>A | ||
| ENST00000494557.2:n.1054G>A | ||
| ENST00000684903.1:c.*920G>A | ENSP00000508612.1:n.*920G>A | |
| ENST00000685348.1:c.*920G>A | ENSP00000510285.1:n.*920G>A | |
| ENST00000685437.1:c.1144G>A | ENSP00000508794.1:p.Asp382Asn | |
| ENST00000685653.1:c.1243G>A | ENSP00000509968.1:p.Asp415Asn | |
| ENST00000685738.1:c.*207G>A | ENSP00000510156.1:n.*207G>A | |
| ENST00000686409.1:n.2294G>A | ||
| ENST00000686455.1:n.1606G>A | ||
| ENST00000686762.1:c.1243G>A | ENSP00000509767.1:p.Asp415Asn | |
| ENST00000687257.1:n.1479G>A | ||
| ENST00000687326.1:c.*177G>A | ENSP00000509665.1:n.*177G>A | |
| ENST00000687505.1:n.1361G>A | ||
| ENST00000687923.1:c.1132G>A | ENSP00000510255.1:p.Asp378Asn | |
| ENST00000687940.1:n.1620G>A | ||
| ENST00000688269.1:n.1839G>A | ||
| ENST00000688326.1:c.676G>A | ||
| ENST00000688444.1:n.1569G>A | ||
| ENST00000688543.1:c.1144G>A | ENSP00000509612.1:p.Asp382Asn | |
| ENST00000688625.1:c.*821G>A | ENSP00000509522.1:n.*821G>A | |
| ENST00000688803.1:n.1474G>A | ||
| ENST00000688914.1:n.229G>A | ||
| ENST00000689097.1:c.*920G>A | ENSP00000509756.1:n.*920G>A | |
| ENST00000689389.1:c.1193+783G>A | ENSP00000510213.1:n.1193+783G>A | |
| ENST00000689418.1:c.*920G>A | ENSP00000509467.1:n.*920G>A | |
| ENST00000689481.1:c.*920G>A | ENSP00000510248.1:n.*920G>A | |
| ENST00000689540.1:n.1393G>A | ||
| ENST00000689876.1:c.1243G>A | ENSP00000508535.1:p.Asp415Asn | |
| ENST00000689914.1:c.*177G>A | ENSP00000509847.1:n.*177G>A | |
| ENST00000690397.1:c.1132G>A | ENSP00000508730.1:p.Asp378Asn | |
| ENST00000690460.1:c.1231G>A | ENSP00000509106.1:p.Asp411Asn | |
| ENST00000690585.1:c.135G>A | ||
| ENST00000690625.1:n.2279G>A | ||
| ENST00000691396.1:c.*1095G>A | ENSP00000510712.1:n.*1095G>A | |
| ENST00000691724.1:c.*200G>A | ENSP00000509255.1:n.*200G>A | |
| ENST00000691779.1:c.*821G>A | ENSP00000508592.1:n.*821G>A | |
| ENST00000691888.1:c.135G>A | ||
| ENST00000691899.1:c.1243G>A | ENSP00000508763.1:p.Asp415Asn | |
| ENST00000692069.1:n.1809G>A | ||
| ENST00000692093.1:c.1144G>A | ENSP00000509669.1:p.Asp382Asn | |
| ENST00000692311.1:n.2067G>A | ||
| ENST00000692558.1:n.1608G>A | ||
| ENST00000692773.1:c.*980G>A | ENSP00000509055.1:n.*980G>A | |
| ENST00000692830.1:c.*988G>A | ENSP00000509461.1:n.*988G>A | |
| ENST00000693069.1:c.*177G>A | ENSP00000510072.1:n.*177G>A | |
| ENST00000693312.1:c.1018G>A | ENSP00000508686.1:p.Asp340Asn | |
| ENST00000693664.1:c.1243G>A | ENSP00000509614.1:p.Asp415Asn | |
| ENST00000693705.1:c.*920G>A | ENSP00000510697.1:n.*920G>A | |
| ENST00000251849.9:c.1243G>A MANE Select | ENSP00000251849.4:p.Asp415Asn | |
| ENST00000442415.7:c.1303G>A | ENSP00000401888.2:p.Asp435Asn | |
| ENST00000251849.8:c.1243G>A | ENSP00000251849.4:p.Asp415Asn | |
| ENST00000423275.5:c.*920G>A | ENSP00000401088.1:n.*920G>A | |
| ENST00000432427.2:c.880G>A | ENSP00000398591.2:p.Asp294Asn | |
| ENST00000442415.6:c.1303G>A | ENSP00000401888.2:p.Asp435Asn | |
| ENST00000460610.1:n.200G>A | ||
| ENST00000465826.5:n.600G>A | ||
| ENST00000475353.1:n.411G>A | ||
| ENST00000494557.1:n.259G>A | ||
| NM_002880.3:c.1243G>A , LRG_413t1:c.1243G>A | NP_002871.1:p.Asp415Asn | |
| XM_005265355.1:c.1243G>A | XP_005265412.1:p.Asp415Asn | |
| XM_005265357.1:c.1144G>A | XP_005265414.1:p.Asp382Asn | |
| XM_005265358.3:c.1000G>A | XP_005265415.1:p.Asp334Asn | |
| XM_005265359.3:c.901G>A | XP_005265416.1:p.Asp301Asn | |
| XM_005265360.1:c.1243G>A | XP_005265417.1:p.Asp415Asn | |
| XM_011533974.1:c.1243G>A | XP_011532276.1:p.Asp415Asn | |
| XM_011533975.1:c.1000G>A | XP_011532277.1:p.Asp334Asn | |
| NM_001354689.1:c.1303G>A | NP_001341618.1:p.Asp435Asn | |
| NM_001354690.1:c.1243G>A | NP_001341619.1:p.Asp415Asn | |
| NM_001354691.1:c.1000G>A | NP_001341620.1:p.Asp334Asn | |
| NM_001354692.1:c.1000G>A | NP_001341621.1:p.Asp334Asn | |
| NM_001354693.1:c.1144G>A | NP_001341622.1:p.Asp382Asn | |
| NM_001354694.1:c.1060G>A | NP_001341623.1:p.Asp354Asn | |
| NM_001354695.1:c.901G>A | NP_001341624.1:p.Asp301Asn | |
| NR_148940.1:n.1771G>A | ||
| NR_148941.1:n.1717G>A | ||
| NR_148942.1:n.1656G>A | ||
| XM_011533974.3:c.1243G>A | XP_011532276.1:p.Asp415Asn | |
| XM_017006966.1:c.1144G>A | XP_016862455.1:p.Asp382Asn | |
| NM_001354689.3:c.1303G>A | NP_001341618.1:p.Asp435Asn | |
| NM_001354690.2:c.1243G>A | NP_001341619.1:p.Asp415Asn | |
| NM_001354691.2:c.1000G>A | NP_001341620.1:p.Asp334Asn | |
| NM_001354692.2:c.1000G>A | NP_001341621.1:p.Asp334Asn | |
| NM_001354693.2:c.1144G>A | NP_001341622.1:p.Asp382Asn | |
| NM_001354694.2:c.1060G>A | NP_001341623.1:p.Asp354Asn | |
| NM_001354695.2:c.901G>A | NP_001341624.1:p.Asp301Asn | |
| NR_148940.2:n.1687G>A | ||
| NR_148941.2:n.1633G>A | ||
| NR_148942.2:n.1572G>A | ||
| NM_001354690.3:c.1243G>A | NP_001341619.1:p.Asp415Asn | |
| NM_001354691.3:c.1000G>A | NP_001341620.1:p.Asp334Asn | |
| NM_001354692.3:c.1000G>A | NP_001341621.1:p.Asp334Asn | |
| NM_001354693.3:c.1144G>A | NP_001341622.1:p.Asp382Asn | |
| NM_001354694.3:c.1060G>A | NP_001341623.1:p.Asp354Asn | |
| NM_001354695.3:c.901G>A | NP_001341624.1:p.Asp301Asn | |
| NM_002880.4:c.1243G>A MANE Select | NP_002871.1:p.Asp415Asn | |
| NR_148940.3:n.1687G>A | ||
| NR_148941.3:n.1633G>A | ||
| NR_148942.3:n.1572G>A |