gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.00000359 (NFE)
Genomes Max Group AF
0.0000117 (NFE)
Exomes Max Group AF
0.00000194 (NFE)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.67802285G>C , CM000676.2:g.67802285G>C | GRCh38 |
| NC_000014.8:g.68269002G>C , CM000676.1:g.68269002G>C | GRCh37 |
| NC_000014.7:g.67338755G>C | NCBI36 |
| NG_011836.1:g.19305C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000347230.9:c.1436-3C>G MANE Select | ENSP00000251119.5:n.1436-3C>G | |
| ENST00000676512.1:c.1436-3C>G | ENSP00000504552.1:n.1436-3C>G | |
| ENST00000676620.1:c.1436-3C>G | ENSP00000504587.1:n.1436-3C>G | |
| ENST00000677026.1:c.1435+1816C>G | ENSP00000503710.1:n.1435+1816C>G | |
| ENST00000678382.1:c.*431-3C>G | ENSP00000504130.1:n.*431-3C>G | |
| ENST00000678386.1:c.1436-3C>G | ENSP00000503677.1:n.1436-3C>G | |
| ENST00000347230.8:c.1436-3C>G | ENSP00000251119.5:n.1436-3C>G | |
| ENST00000554523.5:n.1573-3C>G | ||
| ENST00000554557.5:c.1271+2932C>G | ENSP00000450431.1:n.1271+2932C>G | |
| ENST00000555452.1:c.1436-3C>G | ENSP00000450603.1:n.1436-3C>G | |
| ENST00000557366.5:n.1482-3C>G | ||
| ENST00000557407.1:n.1571-3C>G | ||
| NM_015346.3:c.1436-3C>G | NP_056161.2:n.1436-3C>G | |
| XM_006720093.2:c.1436-3C>G | XP_006720156.1:n.1436-3C>G | |
| XM_011536606.1:c.-74-3C>G | XP_011534908.1:n.-74-3C>G | |
| XM_011536609.1:c.1436-3C>G | XP_011534911.1:n.1436-3C>G | |
| XM_011536609.2:c.1436-3C>G | XP_011534911.1:n.1436-3C>G | |
| XM_017021124.1:c.1436-3C>G | XP_016876613.1:n.1436-3C>G | |
| XM_017021125.1:c.1436-3C>G | XP_016876614.1:n.1436-3C>G | |
| XM_017021126.1:c.-74-3C>G | XP_016876615.1:n.-74-3C>G | |
| NM_015346.4:c.1436-3C>G MANE Select | NP_056161.2:n.1436-3C>G |