gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.00067319 (AFR)
Genomes Max Group AF
0.00055924 (AFR)
Exomes Max Group AF
0.00067006 (AFR)
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.29223410G>A , CM000664.2:g.29223410G>A | GRCh38 |
| NC_000002.11:g.29446276G>A , CM000664.1:g.29446276G>A | GRCh37 |
| NC_000002.10:g.29299780G>A | NCBI36 |
| NG_009445.1:g.703157C>T , LRG_488:g.703157C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000389048.8:c.3291C>T MANE Select | ENSP00000373700.3:p.Cys1097= | |
| ENST00000431873.6:c.518C>T | ||
| ENST00000638605.1:n.168C>T | ||
| ENST00000642122.1:c.87C>T | ENSP00000493203.1:p.Cys29= | |
| ENST00000389048.7:c.3291C>T | ENSP00000373700.3:p.Cys1097= | |
| ENST00000431873.5:c.171C>T | ENSP00000414027.2:p.Cys57= | |
| ENST00000618119.4:c.2160C>T | ENSP00000482733.1:p.Cys720= | |
| NM_004304.4:c.3291C>T | NP_004295.2:p.Cys1097= | |
| NM_001353765.1:c.87C>T | NP_001340694.1:p.Cys29= | |
| XM_024452778.1:c.444C>T | XP_024308546.1:p.Cys148= | |
| XM_024452779.1:c.87C>T | XP_024308547.1:p.Cys29= | |
| NM_004304.5:c.3291C>T MANE Select | NP_004295.2:p.Cys1097= | |
| NM_001353765.2:c.87C>T | NP_001340694.1:p.Cys29= |