Linked Data
ClinVar Variation Id:
280524
dbSNP Id:
rs763559779
ExAC:
3:12653476 A / G
gnomAD v2:
3-12653476-A-G
gnomAD v3:
3-12611977-A-G
gnomAD v4:
3-12611977-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.12611977A>G , CM000665.2:g.12611977A>G | GRCh38 |
| NC_000003.11:g.12653476A>G , CM000665.1:g.12653476A>G | GRCh37 |
| NC_000003.10:g.12628476A>G | NCBI36 |
| NG_007467.1:g.57203T>C , LRG_413:g.57203T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000416093.2:c.261+32T>C | ENSP00000391265.2:n.261+32T>C | |
| ENST00000423275.6:c.208-2642T>C | ENSP00000401088.1:n.208-2642T>C | |
| ENST00000491290.2:n.670T>C | ||
| ENST00000684903.1:c.208-2642T>C | ENSP00000508612.1:n.208-2642T>C | |
| ENST00000685348.1:c.208-2642T>C | ENSP00000510285.1:n.208-2642T>C | |
| ENST00000685437.1:c.293T>C | ENSP00000508794.1:p.Val98Ala | |
| ENST00000685653.1:c.293T>C | ENSP00000509968.1:p.Val98Ala | |
| ENST00000685738.1:c.293T>C | ENSP00000510156.1:p.Val98Ala | |
| ENST00000685740.1:c.293T>C | ENSP00000510566.1:p.Val98Ala | |
| ENST00000685959.1:c.293T>C | ENSP00000510452.1:p.Val98Ala | |
| ENST00000686409.1:n.584T>C | ||
| ENST00000686455.1:n.656T>C | ||
| ENST00000686479.1:n.664T>C | ||
| ENST00000686762.1:c.293T>C | ENSP00000509767.1:p.Val98Ala | |
| ENST00000687257.1:n.628T>C | ||
| ENST00000687326.1:c.293T>C | ENSP00000509665.1:p.Val98Ala | |
| ENST00000687348.1:c.293T>C | ENSP00000509787.1:p.Val98Ala | |
| ENST00000687923.1:c.293T>C | ENSP00000510255.1:p.Val98Ala | |
| ENST00000687940.1:n.670T>C | ||
| ENST00000688269.1:n.592T>C | ||
| ENST00000688444.1:n.619T>C | ||
| ENST00000688543.1:c.293T>C | ENSP00000509612.1:p.Val98Ala | |
| ENST00000688625.1:c.208-2642T>C | ENSP00000509522.1:n.208-2642T>C | |
| ENST00000688753.1:c.293T>C | ENSP00000508771.1:p.Val98Ala | |
| ENST00000688803.1:n.623T>C | ||
| ENST00000689033.1:c.293T>C | ENSP00000508983.1:p.Val98Ala | |
| ENST00000689097.1:c.208-2642T>C | ENSP00000509756.1:n.208-2642T>C | |
| ENST00000689226.1:c.293T>C | ENSP00000510613.1:p.Val98Ala | |
| ENST00000689389.1:c.293T>C | ENSP00000510213.1:p.Val98Ala | |
| ENST00000689418.1:c.208-2642T>C | ENSP00000509467.1:n.208-2642T>C | |
| ENST00000689481.1:c.208-2642T>C | ENSP00000510248.1:n.208-2642T>C | |
| ENST00000689540.1:n.443T>C | ||
| ENST00000689876.1:c.293T>C | ENSP00000508535.1:p.Val98Ala | |
| ENST00000689914.1:c.293T>C | ENSP00000509847.1:p.Val98Ala | |
| ENST00000690397.1:c.293T>C | ENSP00000508730.1:p.Val98Ala | |
| ENST00000690460.1:c.293T>C | ENSP00000509106.1:p.Val98Ala | |
| ENST00000690625.1:n.596T>C | ||
| ENST00000691396.1:c.*86T>C | ENSP00000510712.1:n.*86T>C | |
| ENST00000691718.1:c.293T>C | ENSP00000510160.1:p.Val98Ala | |
| ENST00000691724.1:c.293T>C | ENSP00000509255.1:p.Val98Ala | |
| ENST00000691779.1:c.208-2642T>C | ENSP00000508592.1:n.208-2642T>C | |
| ENST00000691899.1:c.293T>C | ENSP00000508763.1:p.Val98Ala | |
| ENST00000692093.1:c.293T>C | ENSP00000509669.1:p.Val98Ala | |
| ENST00000692311.1:n.666T>C | ||
| ENST00000692558.1:n.658T>C | ||
| ENST00000692773.1:c.208-2642T>C | ENSP00000509055.1:n.208-2642T>C | |
| ENST00000692777.1:n.621T>C | ||
| ENST00000692830.1:c.208-2642T>C | ENSP00000509461.1:n.208-2642T>C | |
| ENST00000692959.1:c.293T>C | ENSP00000509353.1:p.Val98Ala | |
| ENST00000693069.1:c.293T>C | ENSP00000510072.1:p.Val98Ala | |
| ENST00000693312.1:c.68T>C | ENSP00000508686.1:p.Val23Ala | |
| ENST00000693664.1:c.293T>C | ENSP00000509614.1:p.Val98Ala | |
| ENST00000693705.1:c.208-2642T>C | ENSP00000510697.1:n.208-2642T>C | |
| ENST00000251849.9:c.293T>C MANE Select | ENSP00000251849.4:p.Val98Ala | |
| ENST00000442415.7:c.293T>C | ENSP00000401888.2:p.Val98Ala | |
| ENST00000251849.8:c.293T>C | ENSP00000251849.4:p.Val98Ala | |
| ENST00000416093.1:c.208-2642T>C | ENSP00000391265.1:n.208-2642T>C | |
| ENST00000423275.5:c.208-2642T>C | ENSP00000401088.1:n.208-2642T>C | |
| ENST00000432427.2:c.29T>C | ENSP00000398591.2:p.Val10Ala | |
| ENST00000442415.6:c.293T>C | ENSP00000401888.2:p.Val98Ala | |
| ENST00000492690.1:n.25T>C | ||
| NM_002880.3:c.293T>C , LRG_413t1:c.293T>C | NP_002871.1:p.Val98Ala | |
| XM_005265355.1:c.293T>C | XP_005265412.1:p.Val98Ala | |
| XM_005265357.1:c.293T>C | XP_005265414.1:p.Val98Ala | |
| XM_005265358.3:c.78-2642T>C | XP_005265415.1:n.78-2642T>C | |
| XM_005265359.3:c.78-2642T>C | XP_005265416.1:n.78-2642T>C | |
| XM_005265360.1:c.293T>C | XP_005265417.1:p.Val98Ala | |
| XM_011533974.1:c.293T>C | XP_011532276.1:p.Val98Ala | |
| XM_011533975.1:c.78-2642T>C | XP_011532277.1:n.78-2642T>C | |
| NM_001354689.1:c.293T>C | NP_001341618.1:p.Val98Ala | |
| NM_001354690.1:c.293T>C | NP_001341619.1:p.Val98Ala | |
| NM_001354691.1:c.78-2642T>C | NP_001341620.1:n.78-2642T>C | |
| NM_001354692.1:c.78-2642T>C | NP_001341621.1:n.78-2642T>C | |
| NM_001354693.1:c.293T>C | NP_001341622.1:p.Val98Ala | |
| NM_001354694.1:c.78-2642T>C | NP_001341623.1:n.78-2642T>C | |
| NM_001354695.1:c.78-2642T>C | NP_001341624.1:n.78-2642T>C | |
| NR_148940.1:n.708T>C | ||
| NR_148941.1:n.708T>C | ||
| NR_148942.1:n.708T>C | ||
| XM_011533974.3:c.293T>C | XP_011532276.1:p.Val98Ala | |
| XM_017006966.1:c.293T>C | XP_016862455.1:p.Val98Ala | |
| XR_001740227.1:n.624T>C | ||
| NM_001354689.3:c.293T>C | NP_001341618.1:p.Val98Ala | |
| NM_001354690.2:c.293T>C | NP_001341619.1:p.Val98Ala | |
| NM_001354691.2:c.78-2642T>C | NP_001341620.1:n.78-2642T>C | |
| NM_001354692.2:c.78-2642T>C | NP_001341621.1:n.78-2642T>C | |
| NM_001354693.2:c.293T>C | NP_001341622.1:p.Val98Ala | |
| NM_001354694.2:c.78-2642T>C | NP_001341623.1:n.78-2642T>C | |
| NM_001354695.2:c.78-2642T>C | NP_001341624.1:n.78-2642T>C | |
| NR_148940.2:n.624T>C | ||
| NR_148941.2:n.624T>C | ||
| NR_148942.2:n.624T>C | ||
| NM_001354690.3:c.293T>C | NP_001341619.1:p.Val98Ala | |
| NM_001354691.3:c.78-2642T>C | NP_001341620.1:n.78-2642T>C | |
| NM_001354692.3:c.78-2642T>C | NP_001341621.1:n.78-2642T>C | |
| NM_001354693.3:c.293T>C | NP_001341622.1:p.Val98Ala | |
| NM_001354694.3:c.78-2642T>C | NP_001341623.1:n.78-2642T>C | |
| NM_001354695.3:c.78-2642T>C | NP_001341624.1:n.78-2642T>C | |
| NM_002880.4:c.293T>C MANE Select | NP_002871.1:p.Val98Ala | |
| NR_148940.3:n.624T>C | ||
| NR_148941.3:n.624T>C | ||
| NR_148942.3:n.624T>C |