gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.35695705 (SAS)
Genomes Max Group AF
0.35695705 (SAS)
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.3574518C>T , CM000679.2:g.3574518C>T | GRCh38 |
| NC_000017.10:g.3477812C>T , CM000679.1:g.3477812C>T | GRCh37 |
| NC_000017.9:g.3424561C>T | NCBI36 |
| NG_029716.1:g.39894G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000572705.2:c.1781-563G>A MANE Select | ENSP00000459962.1:n.1781-563G>A | |
| ENST00000650505.1:c.*262-563G>A | ENSP00000497337.1:n.*262-563G>A | |
| ENST00000310522.5:c.1601-563G>A | ENSP00000311692.5:n.1601-563G>A | |
| ENST00000399756.8:c.1781-563G>A | ENSP00000382659.4:n.1781-563G>A | |
| ENST00000399759.7:c.1781-563G>A | ENSP00000382661.3:n.1781-563G>A | |
| ENST00000425167.6:c.1814-563G>A | ENSP00000409627.2:n.1814-563G>A | |
| ENST00000570742.1:n.359-563G>A | ||
| ENST00000571088.5:c.1781-563G>A | ENSP00000461007.1:n.1781-563G>A | |
| ENST00000572705.1:c.1781-563G>A | ENSP00000459962.1:n.1781-563G>A | |
| ENST00000574085.5:n.1868-563G>A | ||
| ENST00000576351.5:c.1751-563G>A | ENSP00000459042.1:n.1751-563G>A | |
| NM_018727.5:c.1781-563G>A | NP_061197.4:n.1781-563G>A | |
| NM_080704.3:c.1781-563G>A | NP_542435.2:n.1781-563G>A | |
| NM_080705.3:c.1781-563G>A | NP_542436.2:n.1781-563G>A | |
| NM_080706.3:c.1781-563G>A | NP_542437.2:n.1781-563G>A | |
| NM_080704.4:c.1781-563G>A MANE Select | NP_542435.2:n.1781-563G>A | |
| NM_080705.4:c.1781-563G>A | NP_542436.2:n.1781-563G>A |