gnomAD v3:
gnomAD v4:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10239909C>G , CM000682.2:g.10239909C>G | GRCh38 |
| NC_000020.10:g.10220557C>G , CM000682.1:g.10220557C>G | GRCh37 |
| NC_000020.9:g.10168557C>G | NCBI36 |
| NG_029626.1:g.26081C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000706269.1:c.-64+20696C>G | ENSP00000516314.1:n.-64+20696C>G | |
| ENST00000685131.1:c.-64+1883C>G | ENSP00000508837.1:n.-64+1883C>G | |
| ENST00000687785.1:c.-241-4066C>G | ENSP00000510219.1:n.-241-4066C>G | |
| ENST00000689077.1:n.393-35520C>G | ||
| ENST00000689248.1:n.97-4843C>G | ||
| ENST00000689757.1:c.-109+12471C>G | ENSP00000509312.1:n.-109+12471C>G | |
| ENST00000689858.1:c.-123-4066C>G | ENSP00000510663.1:n.-123-4066C>G | |
| ENST00000690099.1:n.393-35520C>G | ||
| ENST00000690766.1:n.393-35520C>G | ||
| ENST00000690812.1:c.-168-4066C>G | ENSP00000509287.1:n.-168-4066C>G | |
| ENST00000691161.1:c.-64+12471C>G | ENSP00000510109.1:n.-64+12471C>G | |
| ENST00000691353.1:c.-263+20696C>G | ENSP00000509759.1:n.-263+20696C>G | |
| ENST00000691665.1:c.-64+5572C>G | ENSP00000508541.1:n.-64+5572C>G | |
| ENST00000692411.1:c.-149+20932C>G | ENSP00000508939.1:n.-149+20932C>G | |
| ENST00000693325.1:c.-64+12471C>G | ENSP00000510558.1:n.-64+12471C>G | |
| ENST00000693732.1:n.393-35520C>G | ||
| ENST00000254976.7:c.-64+20932C>G MANE Select | ENSP00000254976.3:n.-64+20932C>G | |
| ENST00000254976.6:c.-64+20932C>G | ENSP00000254976.2:n.-64+20932C>G | |
| ENST00000304886.6:c.-64+20932C>G | ENSP00000307341.2:n.-64+20932C>G | |
| ENST00000430336.1:c.-64+20696C>G | ENSP00000400720.1:n.-64+20696C>G | |
| NM_003081.3:c.-64+20932C>G | NP_003072.2:n.-64+20932C>G | |
| NM_130811.2:c.-64+20932C>G | NP_570824.1:n.-64+20932C>G | |
| XM_005260808.3:c.-64+20696C>G | XP_005260865.1:n.-64+20696C>G | |
| XM_005260810.3:c.-64+20696C>G | XP_005260867.1:n.-64+20696C>G | |
| NM_001322902.1:c.-64+20696C>G | NP_001309831.1:n.-64+20696C>G | |
| NM_001322903.1:c.-64+5572C>G | NP_001309832.1:n.-64+5572C>G | |
| NM_001322904.1:c.-64+12471C>G | NP_001309833.1:n.-64+12471C>G | |
| NM_001322905.1:c.-123-4066C>G | NP_001309834.1:n.-123-4066C>G | |
| NM_001322906.1:c.-64+1883C>G | NP_001309835.1:n.-64+1883C>G | |
| NM_001322907.1:c.-64+12471C>G | NP_001309836.1:n.-64+12471C>G | |
| NM_001322908.1:c.-241-4066C>G | NP_001309837.1:n.-241-4066C>G | |
| NM_001322909.1:c.-108-19448C>G | NP_001309838.1:n.-108-19448C>G | |
| NM_001322910.1:c.-64+12471C>G | NP_001309839.1:n.-64+12471C>G | |
| NM_003081.4:c.-64+20932C>G | NP_003072.2:n.-64+20932C>G | |
| NM_130811.3:c.-64+20932C>G | NP_570824.1:n.-64+20932C>G | |
| XM_005260808.5:c.-64+20696C>G | XP_005260865.1:n.-64+20696C>G | |
| XM_017028021.2:c.-123-4066C>G | XP_016883510.1:n.-123-4066C>G | |
| XM_017028022.1:c.-64+1883C>G | XP_016883511.1:n.-64+1883C>G | |
| NM_001322902.2:c.-64+20696C>G | NP_001309831.1:n.-64+20696C>G | |
| NM_001322903.2:c.-64+5572C>G | NP_001309832.1:n.-64+5572C>G | |
| NM_001322904.2:c.-64+12471C>G | NP_001309833.1:n.-64+12471C>G | |
| NM_001322905.2:c.-123-4066C>G | NP_001309834.1:n.-123-4066C>G | |
| NM_001322906.2:c.-64+1883C>G | NP_001309835.1:n.-64+1883C>G | |
| NM_001322907.2:c.-64+12471C>G | NP_001309836.1:n.-64+12471C>G | |
| NM_001322908.2:c.-241-4066C>G | NP_001309837.1:n.-241-4066C>G | |
| NM_001322909.2:c.-108-19448C>G | NP_001309838.1:n.-108-19448C>G | |
| NM_001322910.2:c.-64+12471C>G | NP_001309839.1:n.-64+12471C>G | |
| NM_003081.5:c.-64+20932C>G | NP_003072.2:n.-64+20932C>G | |
| NM_130811.4:c.-64+20932C>G MANE Select | NP_570824.1:n.-64+20932C>G |