ClinVar RCV:
ClinVar Variation:
dbSNP:
gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.00033618 (AFR)
Genomes Max Group AF
0.00029987 (AFR)
Exomes Max Group AF
0.00028038 (AFR)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.31531371C>T , CM000664.2:g.31531371C>T | GRCh38 |
| NC_000002.11:g.31756441C>T , CM000664.1:g.31756441C>T | GRCh37 |
| NC_000002.10:g.31609945C>T | NCBI36 |
| NG_008365.1:g.54601G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000622030.2:c.547G>A MANE Select | ENSP00000477587.1:p.Gly183Ser | |
| ENST00000622030.1:c.547G>A | ENSP00000477587.1:p.Gly183Ser | |
| NM_000348.3:c.547G>A | NP_000339.2:p.Gly183Ser | |
| XM_011533069.1:c.325G>A | XP_011531371.1:p.Gly109Ser | |
| XM_011533070.1:c.292G>A | XP_011531372.1:p.Gly98Ser | |
| XM_011533071.1:c.292G>A | XP_011531373.1:p.Gly98Ser | |
| XM_011533072.1:c.292G>A | XP_011531374.1:p.Gly98Ser | |
| XM_011533069.2:c.325G>A | XP_011531371.1:p.Gly109Ser | |
| XM_011533072.2:c.292G>A | XP_011531374.1:p.Gly98Ser | |
| NM_000348.4:c.547G>A MANE Select | NP_000339.2:p.Gly183Ser |