ClinVar Variation:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.00001062 (AFR)
Exomes Max Group AF
0.00002376 (AFR)
MyVariant.info:
GRCh38
chr9:g.133352058C>T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133352058C>T , CM000671.2:g.133352058C>T | GRCh38 |
| NC_000009.10:g.135208734C>T | NCBI36 |
| NG_008477.1:g.9449G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371974.8:c.833+3G>A MANE Select | ENSP00000361042.3:n.833+3G>A | |
| ENST00000371974.7:c.833+3G>A | ENSP00000361042.3:n.833+3G>A | |
| ENST00000437995.1:n.743+3G>A | ||
| ENST00000495952.5:n.823+3G>A | ||
| ENST00000615505.4:c.506+3G>A | ENSP00000482067.1:n.506+3G>A | |
| NM_001280787.1:c.506+3G>A | NP_001267716.1:n.506+3G>A | |
| NM_003172.3:c.833+3G>A | NP_003163.1:n.833+3G>A | |
| XM_011518942.1:c.506+3G>A | XP_011517244.1:n.506+3G>A | |
| NM_003172.4:c.833+3G>A MANE Select | NP_003163.1:n.833+3G>A |