ClinVar Variation:
dbSNP:
gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.00016486 (NFE)
Genomes Max Group AF
0.00003762 (NFE)
Exomes Max Group AF
0.00016961 (NFE)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.63942820G>A , CM000679.2:g.63942820G>A | GRCh38 |
| NC_000017.10:g.62020180G>A , CM000679.1:g.62020180G>A | GRCh37 |
| NC_000017.9:g.59373912G>A | NCBI36 |
| NG_011699.1:g.35099C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000435607.3:c.4288+6C>T MANE Select | ENSP00000396320.1:n.4288+6C>T | |
| ENST00000578147.5:c.4288+6C>T | ENSP00000463963.1:n.4288+6C>T | |
| NM_000334.4:c.4288+6C>T MANE Select | NP_000325.4:n.4288+6C>T | |
| XM_005257566.3:c.4288+6C>T | XP_005257623.1:n.4288+6C>T |