ClinVar Variation:
dbSNP:
gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.0001596 (NFE)
Genomes Max Group AF
0.00006804 (NFE)
Exomes Max Group AF
0.00016117 (NFE)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.17114175G>A , CM000672.2:g.17114175G>A | GRCh38 |
| NC_000010.10:g.17156174G>A , CM000672.1:g.17156174G>A | GRCh37 |
| NC_000010.9:g.17196180G>A | NCBI36 |
| NG_008967.1:g.20643C>T , LRG_540:g.20643C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000377833.10:c.735C>T MANE Select | ENSP00000367064.4:p.Cys245= | |
| ENST00000377833.8:c.735C>T | ENSP00000367064.4:p.Cys245= | |
| NM_001081.3:c.735C>T , LRG_540t1:c.735C>T | NP_001072.2:p.Cys245= | |
| XM_011519708.1:c.735C>T | XP_011518010.1:p.Cys245= | |
| XM_011519708.2:c.735C>T | XP_011518010.1:p.Cys245= | |
| NM_001081.4:c.735C>T MANE Select | NP_001072.2:p.Cys245= |