gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.06418121 (NFE)
Genomes Max Group AF
0.06418121 (NFE)
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.143286187T>C , CM000665.2:g.143286187T>C | GRCh38 |
| NC_000003.11:g.143005029T>C , CM000665.1:g.143005029T>C | GRCh37 |
| NC_000003.10:g.144487719T>C | NCBI36 |
| NG_017077.1:g.567345A>G | |
| NG_017077.2:g.567345A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000316549.11:c.1605-17207A>G MANE Select | ENSP00000320246.6:n.1605-17207A>G | |
| ENST00000316549.10:c.1605-17207A>G | ENSP00000320246.6:n.1605-17207A>G | |
| NM_173653.3:c.1605-17207A>G | NP_775924.1:n.1605-17207A>G | |
| XM_011512703.1:c.957-17207A>G | XP_011511005.1:n.957-17207A>G | |
| XM_011512703.3:c.957-17207A>G | XP_011511005.1:n.957-17207A>G | |
| XM_017006202.2:c.1712-1845A>G | XP_016861691.1:n.1712-1845A>G | |
| XM_017006203.1:c.1254-17207A>G | XP_016861692.1:n.1254-17207A>G | |
| NM_173653.4:c.1605-17207A>G MANE Select | NP_775924.1:n.1605-17207A>G |