gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.00013381 (MID)
Genomes Max Group AF
0.00004739 (AFR)
Exomes Max Group AF
0.00014155 (MID)
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.50198448G>A , CM000679.2:g.50198448G>A | GRCh38 |
| NC_000017.10:g.48275809G>A , CM000679.1:g.48275809G>A | GRCh37 |
| NC_000017.9:g.45630808G>A | NCBI36 |
| NG_007400.1:g.8192C>T , LRG_1:g.8192C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000225964.10:c.528C>T MANE Select | ENSP00000225964.6:p.Ser176= | |
| ENST00000225964.9:c.528C>T | ENSP00000225964.5:p.Ser176= | |
| ENST00000495677.1:n.255C>T | ||
| NM_000088.3:c.528C>T , LRG_1t1:c.528C>T | NP_000079.2:p.Ser176= | |
| XM_005257058.3:c.528C>T | XP_005257115.2:p.Ser176= | |
| XM_005257059.3:c.528C>T | XP_005257116.2:p.Ser176= | |
| XM_011524341.1:c.528C>T | XP_011522643.1:p.Ser176= | |
| XM_005257058.4:c.528C>T | XP_005257115.2:p.Ser176= | |
| XM_005257059.4:c.528C>T | XP_005257116.2:p.Ser176= | |
| NM_000088.4:c.528C>T MANE Select | NP_000079.2:p.Ser176= |