gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.00000505 (NFE)
Exomes Max Group AF
0.0000046 (NFE)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.89943364G>A , CM000670.2:g.89943364G>A | GRCh38 |
| NC_000008.10:g.90955592G>A , CM000670.1:g.90955592G>A | GRCh37 |
| NC_000008.9:g.91024768G>A | NCBI36 |
| NG_008860.1:g.46308C>T , LRG_158:g.46308C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000494804.2:n.3375C>T | ||
| ENST00000517337.2:c.1827C>T | ENSP00000429971.2:p.Val609= | |
| ENST00000523444.2:c.1827C>T | ENSP00000428252.2:p.Val609= | |
| ENST00000697292.1:c.2073C>T | ENSP00000513229.1:p.Val691= | |
| ENST00000697293.1:c.2073C>T | ENSP00000513230.1:p.Val691= | |
| ENST00000697294.1:c.*1684C>T | ENSP00000513231.1:n.*1684C>T | |
| ENST00000697295.1:c.*1382C>T | ENSP00000513232.1:n.*1382C>T | |
| ENST00000697296.1:c.*1741C>T | ENSP00000513233.1:n.*1741C>T | |
| ENST00000697297.1:n.3858C>T | ||
| ENST00000697298.1:c.1827C>T | ENSP00000513234.1:p.Val609= | |
| ENST00000697299.1:c.1827C>T | ENSP00000513235.1:p.Val609= | |
| ENST00000697300.1:c.*1677C>T | ENSP00000513236.1:n.*1677C>T | |
| ENST00000697301.1:c.*1594C>T | ENSP00000513237.1:n.*1594C>T | |
| ENST00000697302.1:c.*1594C>T | ENSP00000513238.1:n.*1594C>T | |
| ENST00000697303.1:c.*1677C>T | ENSP00000513239.1:n.*1677C>T | |
| ENST00000697304.1:c.1761C>T | ENSP00000513240.1:p.Val587= | |
| ENST00000697305.1:n.2340C>T | ||
| ENST00000697306.1:c.*2624C>T | ENSP00000513241.1:n.*2624C>T | |
| ENST00000697307.1:c.1848C>T | ENSP00000513242.1:p.Val616= | |
| ENST00000697308.1:c.2004C>T | ENSP00000513243.1:p.Val668= | |
| ENST00000697309.1:c.2073C>T | ENSP00000513244.1:p.Val691= | |
| ENST00000697310.1:c.2073C>T | ENSP00000513245.1:p.Val691= | |
| ENST00000697311.1:c.2073C>T | ENSP00000513246.1:p.Val691= | |
| ENST00000697312.1:c.*1471C>T | ENSP00000513247.1:n.*1471C>T | |
| ENST00000697313.1:n.2688-7752C>T | ||
| ENST00000697314.1:n.3637-7752C>T | ||
| ENST00000697315.1:c.2073C>T | ENSP00000513248.1:p.Val691= | |
| ENST00000697316.1:n.2194C>T | ||
| ENST00000265433.8:c.2073C>T MANE Select | ENSP00000265433.4:p.Val691= | |
| ENST00000265433.7:c.2073C>T | ENSP00000265433.3:p.Val691= | |
| ENST00000396252.6:c.*1946C>T | ENSP00000379551.2:n.*1946C>T | |
| ENST00000409330.5:c.1827C>T | ENSP00000386924.1:p.Val609= | |
| ENST00000520325.1:n.489C>T | ||
| ENST00000613033.1:c.183C>T | ENSP00000484487.1:p.Val61= | |
| NM_001024688.2:c.1827C>T | NP_001019859.1:p.Val609= | |
| NM_002485.4:c.2073C>T , LRG_158t1:c.2073C>T | NP_002476.2:p.Val691= | |
| XM_011517044.1:c.2049C>T | XP_011515346.1:p.Val683= | |
| XM_011517045.1:c.1827C>T | XP_011515347.1:p.Val609= | |
| XM_017013460.1:c.1194C>T | XP_016868949.1:p.Val398= | |
| XM_017013462.2:c.1194C>T | XP_016868951.1:p.Val398= | |
| XM_024447163.1:c.1827C>T | XP_024302931.1:p.Val609= | |
| XM_024447164.1:c.1827C>T | XP_024302932.1:p.Val609= | |
| XM_024447165.1:c.1194C>T | XP_024302933.1:p.Val398= | |
| NM_002485.5:c.2073C>T MANE Select | NP_002476.2:p.Val691= | |
| NM_001024688.3:c.1827C>T | NP_001019859.1:p.Val609= |