gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.55893358 (EAS)
Genomes Max Group AF
0.55893358 (EAS)
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.162427897G>A , CM000668.2:g.162427897G>A | GRCh38 |
| NC_000006.11:g.162848929G>A , CM000668.1:g.162848929G>A | GRCh37 |
| NC_000006.10:g.162768919G>A | NCBI36 |
| NG_008289.1:g.304906C>T | |
| NG_008289.2:g.304906C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000338468.8:c.171+15413C>T | ENSP00000343589.4:n.171+15413C>T | |
| ENST00000366894.6:c.171+15413C>T | ENSP00000355860.2:n.171+15413C>T | |
| ENST00000366898.6:c.171+15413C>T MANE Select | ENSP00000355865.1:n.171+15413C>T | |
| ENST00000673871.1:c.166+15413C>T | ||
| ENST00000674232.1:n.189+15413C>T | ||
| ENST00000674259.1:n.228+15413C>T | ||
| ENST00000674493.1:n.188+15413C>T | ||
| ENST00000674501.1:n.278+15413C>T | ||
| ENST00000338468.7:c.-281+15413C>T | ENSP00000343589.3:n.-281+15413C>T | |
| ENST00000366892.5:c.171+15413C>T | ENSP00000355858.1:n.171+15413C>T | |
| ENST00000366894.5:c.-162+15413C>T | ENSP00000355860.1:n.-162+15413C>T | |
| ENST00000366896.5:c.171+15413C>T | ENSP00000355862.1:n.171+15413C>T | |
| ENST00000366897.5:c.171+15413C>T | ENSP00000355863.1:n.171+15413C>T | |
| ENST00000366898.5:c.171+15413C>T | ENSP00000355865.1:n.171+15413C>T | |
| ENST00000479615.5:c.-66-165132C>T | ENSP00000434414.1:n.-66-165132C>T | |
| NM_004562.2:c.171+15413C>T | NP_004553.2:n.171+15413C>T | |
| NM_013987.2:c.171+15413C>T | NP_054642.2:n.171+15413C>T | |
| NM_013988.2:c.171+15413C>T | NP_054643.2:n.171+15413C>T | |
| XM_011535863.1:c.171+15413C>T | XP_011534165.1:n.171+15413C>T | |
| XM_011535864.1:c.171+15413C>T | XP_011534166.1:n.171+15413C>T | |
| XM_011535865.1:c.171+15413C>T | XP_011534167.1:n.171+15413C>T | |
| XM_011535866.1:c.171+15413C>T | XP_011534168.1:n.171+15413C>T | |
| XM_011535867.1:c.171+15413C>T | XP_011534169.1:n.171+15413C>T | |
| XM_017010908.1:c.285+15413C>T | XP_016866397.1:n.285+15413C>T | |
| XM_017010909.2:c.-66-165132C>T | XP_016866398.1:n.-66-165132C>T | |
| XM_024446449.1:c.-66-165132C>T | XP_024302217.1:n.-66-165132C>T | |
| XR_001743443.2:n.277+15413C>T | ||
| NM_004562.3:c.171+15413C>T MANE Select | NP_004553.2:n.171+15413C>T | |
| NM_013987.3:c.171+15413C>T | NP_054642.2:n.171+15413C>T | |
| NM_013988.3:c.171+15413C>T | NP_054643.2:n.171+15413C>T |