gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.1637583 (NFE)
Genomes Max Group AF
0.1637583 (NFE)
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.15893561A>T , CM000681.2:g.15893561A>T | GRCh38 |
| NC_000019.9:g.16004371A>T , CM000681.1:g.16004371A>T | GRCh37 |
| NC_000019.8:g.15865371A>T | NCBI36 |
| NG_007971.2:g.9514T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000221700.11:c.344-979T>A MANE Select | ENSP00000221700.3:n.344-979T>A | |
| ENST00000011989.11:c.343+176T>A | ENSP00000011989.8:n.343+176T>A | |
| ENST00000221700.10:c.344-979T>A | ENSP00000221700.3:n.344-979T>A | |
| ENST00000392846.7:n.195-979T>A | ||
| ENST00000586927.2:c.344-979T>A | ENSP00000465514.1:n.344-979T>A | |
| ENST00000587671.2:c.199-979T>A | ENSP00000467443.2:n.199-979T>A | |
| ENST00000608168.1:n.397-979T>A | ||
| NM_001082.4:c.344-979T>A | NP_001073.3:n.344-979T>A | |
| NM_001082.5:c.344-979T>A MANE Select | NP_001073.3:n.344-979T>A |