gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.00256339 (AFR)
Genomes Max Group AF
0.00215545 (AFR)
Exomes Max Group AF
0.00278857 (AFR)
ClinVar Allele:
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.25814172C>T , CM000663.2:g.25814172C>T | GRCh38 |
| NC_000001.10:g.26140663C>T , CM000663.1:g.26140663C>T | GRCh37 |
| NC_000001.9:g.26013250C>T | NCBI36 |
| NG_009930.1:g.18997C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000354177.9:c.1425C>T | ENSP00000346109.5:p.Gly475= | |
| ENST00000494537.2:c.1583C>T | ENSP00000508308.1:n.1583C>T | |
| ENST00000361547.7:c.1596C>T MANE Select | ENSP00000355141.2:p.Gly532= | |
| ENST00000354177.8:c.1494C>T | ENSP00000346109.4:p.Gly498= | |
| ENST00000361547.6:c.1596C>T | ENSP00000355141.2:p.Gly532= | |
| ENST00000374315.1:c.1494C>T | ENSP00000363434.1:p.Gly498= | |
| ENST00000494537.1:n.363C>T | ||
| ENST00000527604.1:c.117C>T | ENSP00000457066.1:p.Gly39= | |
| ENST00000559265.1:n.255+2293C>T | ||
| ENST00000630065.2:c.24C>T | ENSP00000487549.1:p.Gly8= | |
| NM_020451.2:c.1596C>T | NP_065184.2:p.Gly532= | |
| NM_206926.1:c.1494C>T | NP_996809.1:p.Gly498= | |
| NM_020451.3:c.1596C>T MANE Select | NP_065184.2:p.Gly532= | |
| NM_206926.2:c.1494C>T | NP_996809.1:p.Gly498= |