Linked Data
dbSNP Id:
rs1484366681
gnomAD v2:
12-28569715-G-A
gnomAD v3:
12-28416782-G-A
gnomAD v4:
12-28416782-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.28416782G>A , CM000674.2:g.28416782G>A | GRCh38 |
| NC_000012.11:g.28569715G>A , CM000674.1:g.28569715G>A | GRCh37 |
| NC_000012.10:g.28460982G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000536442.6:c.762+25371G>A MANE Select | ENSP00000445660.2:n.762+25371G>A | |
| ENST00000381259.5:c.762+25371G>A | ENSP00000370658.1:n.762+25371G>A | |
| ENST00000535520.5:c.*680+25371G>A | ENSP00000438558.1:n.*680+25371G>A | |
| ENST00000536154.5:c.-18-33379G>A | ENSP00000444440.1:n.-18-33379G>A | |
| ENST00000536442.5:c.762+25371G>A | ENSP00000445660.1:n.762+25371G>A | |
| ENST00000539107.5:c.655-33379G>A | ENSP00000440513.1:n.655-33379G>A | |
| ENST00000539904.1:n.890+25371G>A | ||
| ENST00000540401.5:n.854+25371G>A | ||
| ENST00000540794.5:c.150+25371G>A | ENSP00000441714.1:n.150+25371G>A | |
| ENST00000543809.5:c.*143+3844G>A | ENSP00000441651.1:n.*143+3844G>A | |
| ENST00000545336.5:c.762+25371G>A | ENSP00000438040.1:n.762+25371G>A | |
| ENST00000545737.5:c.762+25371G>A | ENSP00000442544.1:n.762+25371G>A | |
| NM_018318.3:c.762+25371G>A | NP_060788.3:n.762+25371G>A | |
| XM_005253413.1:c.762+25371G>A | XP_005253470.1:n.762+25371G>A | |
| XM_005253414.1:c.762+25371G>A | XP_005253471.1:n.762+25371G>A | |
| XM_005253415.1:c.672+25371G>A | XP_005253472.1:n.672+25371G>A | |
| XM_006719103.2:c.786+25371G>A | XP_006719166.1:n.786+25371G>A | |
| XM_006719104.2:c.762+25371G>A | XP_006719167.1:n.762+25371G>A | |
| XM_006719105.1:c.762+25371G>A | XP_006719168.1:n.762+25371G>A | |
| XM_011520728.1:c.762+25371G>A | XP_011519030.1:n.762+25371G>A | |
| XM_011520729.1:c.762+25371G>A | XP_011519031.1:n.762+25371G>A | |
| XM_011520730.1:c.762+25371G>A | XP_011519032.1:n.762+25371G>A | |
| XM_011520731.1:c.759+25371G>A | XP_011519033.1:n.759+25371G>A | |
| XM_011520732.1:c.672+25371G>A | XP_011519034.1:n.672+25371G>A | |
| XM_011520733.1:c.645+25371G>A | XP_011519035.1:n.645+25371G>A | |
| XM_011520734.1:c.276+25371G>A | XP_011519036.1:n.276+25371G>A | |
| XM_011520735.1:c.276+25371G>A | XP_011519037.1:n.276+25371G>A | |
| NM_001330367.1:c.655-33379G>A | NP_001317296.1:n.655-33379G>A | |
| NM_001352078.1:c.762+25371G>A | NP_001339007.1:n.762+25371G>A | |
| NM_001352079.1:c.762+25371G>A | NP_001339008.1:n.762+25371G>A | |
| NM_001352080.1:c.762+25371G>A | NP_001339009.1:n.762+25371G>A | |
| NM_001352081.1:c.762+25371G>A | NP_001339010.1:n.762+25371G>A | |
| NM_001352082.1:c.735+25371G>A | NP_001339011.1:n.735+25371G>A | |
| NM_001352083.1:c.735+25371G>A | NP_001339012.1:n.735+25371G>A | |
| NM_001352084.1:c.684+25371G>A | NP_001339013.1:n.684+25371G>A | |
| NM_001352086.1:c.672+25371G>A | NP_001339015.1:n.672+25371G>A | |
| NM_001352087.1:c.276+25371G>A | NP_001339016.1:n.276+25371G>A | |
| NM_018318.4:c.762+25371G>A | NP_060788.3:n.762+25371G>A | |
| XM_006719104.3:c.762+25371G>A | XP_006719167.1:n.762+25371G>A | |
| XM_017019569.1:c.762+25371G>A | XP_016875058.1:n.762+25371G>A | |
| XM_017019572.1:c.735+25371G>A | XP_016875061.1:n.735+25371G>A | |
| XM_017019574.2:c.672+25371G>A | XP_016875063.1:n.672+25371G>A | |
| XM_024449032.1:c.762+25371G>A | XP_024304800.1:n.762+25371G>A | |
| XM_024449033.1:c.762+25371G>A | XP_024304801.1:n.762+25371G>A | |
| XM_024449034.1:c.762+25371G>A | XP_024304802.1:n.762+25371G>A | |
| XM_024449035.1:c.645+25371G>A | XP_024304803.1:n.645+25371G>A | |
| XM_024449036.1:c.735+25371G>A | XP_024304804.1:n.735+25371G>A | |
| XM_024449037.1:c.735+25371G>A | XP_024304805.1:n.735+25371G>A | |
| XM_024449038.1:c.565-33379G>A | XP_024304806.1:n.565-33379G>A | |
| XM_024449039.1:c.672+25371G>A | XP_024304807.1:n.672+25371G>A | |
| NM_001330367.2:c.655-33379G>A | NP_001317296.1:n.655-33379G>A | |
| NM_001352078.2:c.762+25371G>A | NP_001339007.1:n.762+25371G>A | |
| NM_001352079.2:c.762+25371G>A | NP_001339008.1:n.762+25371G>A | |
| NM_001352080.2:c.762+25371G>A | NP_001339009.1:n.762+25371G>A | |
| NM_001352081.2:c.762+25371G>A | NP_001339010.1:n.762+25371G>A | |
| NM_001352082.2:c.735+25371G>A | NP_001339011.1:n.735+25371G>A | |
| NM_001352083.2:c.735+25371G>A | NP_001339012.1:n.735+25371G>A | |
| NM_001352084.2:c.684+25371G>A | NP_001339013.1:n.684+25371G>A | |
| NM_001352086.2:c.672+25371G>A | NP_001339015.1:n.672+25371G>A | |
| NM_001352087.2:c.276+25371G>A | NP_001339016.1:n.276+25371G>A | |
| NM_018318.5:c.762+25371G>A MANE Select | NP_060788.3:n.762+25371G>A | |
| NM_001387000.1:c.762+25371G>A | NP_001373929.1:n.762+25371G>A |