gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.00001545 (NFE)
Genomes Max Group AF
0.00001171 (NFE)
Exomes Max Group AF
0.00001389 (NFE)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.50188099G>A , CM000679.2:g.50188099G>A | GRCh38 |
| NC_000017.10:g.48265460G>A , CM000679.1:g.48265460G>A | GRCh37 |
| NC_000017.9:g.45620459G>A | NCBI36 |
| NG_007400.1:g.18541C>T , LRG_1:g.18541C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000225964.10:c.3258C>T MANE Select | ENSP00000225964.6:p.Pro1086= | |
| ENST00000225964.9:c.3258C>T | ENSP00000225964.5:p.Pro1086= | |
| ENST00000486572.1:n.456C>T | ||
| ENST00000511732.1:n.582C>T | ||
| NM_000088.3:c.3258C>T , LRG_1t1:c.3258C>T | NP_000079.2:p.Pro1086= | |
| XM_005257058.3:c.2988C>T | XP_005257115.2:p.Pro996= | |
| XM_005257059.3:c.2340C>T | XP_005257116.2:p.Pro780= | |
| XM_011524341.1:c.3060C>T | XP_011522643.1:p.Pro1020= | |
| XM_005257058.4:c.2988C>T | XP_005257115.2:p.Pro996= | |
| XM_005257059.4:c.2340C>T | XP_005257116.2:p.Pro780= | |
| NM_000088.4:c.3258C>T MANE Select | NP_000079.2:p.Pro1086= |