gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.00081713 (AFR)
Genomes Max Group AF
0.0007262 (AFR)
Exomes Max Group AF
0.00077228 (AFR)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.129369975C>T , CM000668.2:g.129369975C>T | GRCh38 |
| NC_000006.11:g.129691120C>T , CM000668.1:g.129691120C>T | GRCh37 |
| NC_000006.10:g.129732813C>T | NCBI36 |
| NG_008678.1:g.491835C>T , LRG_409:g.491835C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000617695.5:c.4944C>T | ENSP00000481744.2:p.Asn1648= | |
| ENST00000618192.5:c.5208C>T | ENSP00000480802.2:p.Asn1736= | |
| ENST00000687590.1:n.1364C>T | ||
| ENST00000421865.3:c.4944C>T MANE Select | ENSP00000400365.2:p.Asn1648= | |
| ENST00000421865.2:c.4944C>T | ENSP00000400365.2:p.Asn1648= | |
| ENST00000617695.4:c.4944C>T | ENSP00000481744.1:p.Asn1648= | |
| ENST00000618192.4:c.4944C>T | ENSP00000480802.1:p.Asn1648= | |
| NM_000426.3:c.4944C>T , LRG_409t1:c.4944C>T | NP_000417.2:p.Asn1648= | |
| NM_001079823.1:c.4944C>T | NP_001073291.1:p.Asn1648= | |
| XM_005266981.2:c.5208C>T | XP_005267038.1:p.Asn1736= | |
| XM_005266982.2:c.5208C>T | XP_005267039.1:p.Asn1736= | |
| XM_011535820.1:c.5208C>T | XP_011534122.1:p.Asn1736= | |
| XM_005266981.3:c.5208C>T | XP_005267038.1:p.Asn1736= | |
| XM_005266982.3:c.5208C>T | XP_005267039.1:p.Asn1736= | |
| XM_011535820.2:c.5208C>T | XP_011534122.1:p.Asn1736= | |
| XM_017010851.2:c.5214C>T | XP_016866340.1:p.Asn1738= | |
| XM_017010852.1:c.3339C>T | XP_016866341.1:p.Asn1113= | |
| XM_017010853.1:c.5208C>T | XP_016866342.1:p.Asn1736= | |
| NM_000426.4:c.4944C>T MANE Select | NP_000417.3:p.Asn1648= | |
| NM_001079823.2:c.4944C>T | NP_001073291.2:p.Asn1648= |