gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.61298923 (EAS)
Genomes Max Group AF
0.62080208 (EAS)
Exomes Max Group AF
0.60991847 (EAS)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.104779988T>A , CM000676.2:g.104779988T>A | GRCh38 |
| NC_000014.8:g.105246325T>A , CM000676.1:g.105246325T>A | GRCh37 |
| NC_000014.7:g.104317370T>A | NCBI36 |
| NG_012188.1:g.20757A>T , LRG_721:g.20757A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000554192.6:c.175+100A>T | ENSP00000450681.3:n.175+100A>T | |
| ENST00000554585.6:c.175+100A>T | ENSP00000481526.2:n.175+100A>T | |
| ENST00000555458.6:c.175+100A>T | ENSP00000451470.3:n.175+100A>T | |
| ENST00000553797.2:c.175+100A>T | ENSP00000507566.1:n.175+100A>T | |
| ENST00000554826.2:n.313+100A>T | ||
| ENST00000610370.2:n.313+100A>T | ||
| ENST00000682269.1:n.692+100A>T | ||
| ENST00000683722.1:c.175+100A>T | ENSP00000507879.1:n.175+100A>T | |
| ENST00000407796.7:c.175+100A>T | ENSP00000384293.2:n.175+100A>T | |
| ENST00000649815.2:c.175+100A>T MANE Select | ENSP00000497822.1:n.175+100A>T | |
| ENST00000349310.7:c.175+100A>T | ENSP00000270202.4:n.175+100A>T | |
| ENST00000402615.6:c.175+100A>T | ENSP00000385326.2:n.175+100A>T | |
| ENST00000407796.6:c.175+100A>T | ENSP00000384293.2:n.175+100A>T | |
| ENST00000554581.5:c.175+100A>T | ENSP00000451828.1:n.175+100A>T | |
| ENST00000554848.5:c.175+100A>T | ENSP00000451166.1:n.175+100A>T | |
| ENST00000555380.1:n.206+100A>T | ||
| ENST00000555528.5:c.175+100A>T | ENSP00000450688.1:n.175+100A>T | |
| ENST00000555926.1:c.175+100A>T | ENSP00000451824.1:n.175+100A>T | |
| NM_001014431.1:c.175+100A>T | NP_001014431.1:n.175+100A>T | |
| NM_001014432.1:c.175+100A>T , LRG_721t1:c.175+100A>T | NP_001014432.1:n.175+100A>T | |
| NM_005163.2:c.175+100A>T , LRG_721t2:c.175+100A>T | NP_005154.2:n.175+100A>T | |
| XM_005267401.1:c.175+100A>T | XP_005267458.1:n.175+100A>T | |
| XM_011536543.1:c.175+100A>T | XP_011534845.1:n.175+100A>T | |
| XM_011536544.1:c.175+100A>T | XP_011534846.1:n.175+100A>T | |
| XR_002957536.1:n.375+100A>T | ||
| NM_001014431.2:c.175+100A>T | NP_001014431.1:n.175+100A>T | |
| NM_001014432.2:c.175+100A>T | NP_001014432.1:n.175+100A>T | |
| NM_001382430.1:c.175+100A>T MANE Select | NP_001369359.1:n.175+100A>T | |
| NM_001382431.1:c.175+100A>T | NP_001369360.1:n.175+100A>T | |
| NM_001382432.1:c.175+100A>T | NP_001369361.1:n.175+100A>T | |
| NM_001382433.1:c.175+100A>T | NP_001369362.1:n.175+100A>T |