ClinVar RCV:
ClinVar Variation:
COSMIC:
COSM5020955
COSM5020956
dbSNP:
gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.28484387 (AFR)
Genomes Max Group AF
0.28118608 (AFR)
Exomes Max Group AF
0.28642335 (AFR)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.32434752G>A , CM000673.2:g.32434752G>A | GRCh38 |
| NC_000011.9:g.32456298G>A , CM000673.1:g.32456298G>A | GRCh37 |
| NC_000011.8:g.32412874G>A | NCBI36 |
| NG_009272.1:g.5790C>T , LRG_525:g.5790C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000332351.9:c.609C>T | ENSP00000331327.5:p.Asn203= | |
| ENST00000379077.9:c.609C>T | ENSP00000368368.5:p.Asn203= | |
| ENST00000448076.9:c.609C>T | ENSP00000413452.5:p.Asn203= | |
| ENST00000452863.10:c.609C>T MANE Select | ENSP00000415516.5:p.Asn203= | |
| ENST00000639563.3:c.609C>T | ENSP00000492269.3:p.Asn203= | |
| ENST00000332351.7:c.594C>T | ENSP00000331327.3:p.Asn198= | |
| ENST00000379077.7:c.594C>T | ENSP00000368368.3:p.Asn198= | |
| ENST00000448076.7:c.594C>T | ENSP00000413452.3:p.Asn198= | |
| ENST00000452863.7:c.594C>T | ENSP00000415516.3:p.Asn198= | |
| NM_000378.4:c.594C>T | NP_000369.3:p.Asn198= | |
| NM_024424.3:c.594C>T | NP_077742.2:p.Asn198= | |
| NM_024426.4:c.594C>T | NP_077744.3:p.Asn198= | |
| NM_000378.5:c.609C>T | NP_000369.4:p.Asn203= | |
| NM_024424.4:c.609C>T | NP_077742.3:p.Asn203= | |
| NM_024426.5:c.609C>T | NP_077744.4:p.Asn203= | |
| NR_160306.1:n.788C>T | ||
| NM_000378.6:c.609C>T | NP_000369.4:p.Asn203= | |
| NM_024424.5:c.609C>T | NP_077742.3:p.Asn203= | |
| NM_024426.6:c.609C>T MANE Select | NP_077744.4:p.Asn203= |