dbSNP:
gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.1563837 (NFE)
Genomes Max Group AF
0.1563837 (NFE)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.65438688T>G , CM000674.2:g.65438688T>G | GRCh38 |
| NC_000012.11:g.65832468T>G , CM000674.1:g.65832468T>G | GRCh37 |
| NC_000012.10:g.64118735T>G | NCBI36 |
| NG_023441.1:g.165046T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000308259.10:c.293-15040T>G MANE Select | ENSP00000312274.6:n.293-15040T>G | |
| ENST00000355192.8:c.314-15040T>G | ENSP00000347324.3:n.314-15040T>G | |
| ENST00000642404.1:c.293-15040T>G | ENSP00000496008.1:n.293-15040T>G | |
| ENST00000642411.1:c.293-15040T>G | ENSP00000494265.1:n.293-15040T>G | |
| ENST00000646299.1:c.293-15040T>G | ENSP00000494941.1:n.293-15040T>G | |
| ENST00000647481.1:c.98-15040T>G | ENSP00000496162.1:n.98-15040T>G | |
| ENST00000308259.9:c.293-15040T>G | ENSP00000312274.5:n.293-15040T>G | |
| ENST00000355192.7:c.314-15040T>G | ENSP00000347324.3:n.314-15040T>G | |
| ENST00000446731.2:c.168-15040T>G | ||
| ENST00000535143.1:n.132-15040T>G | ||
| ENST00000535239.5:c.293-15040T>G | ENSP00000445843.1:n.293-15040T>G | |
| ENST00000535664.5:c.293-15040T>G | ENSP00000441650.1:n.293-15040T>G | |
| ENST00000538045.5:c.293-15040T>G | ENSP00000442620.1:n.293-15040T>G | |
| ENST00000540804.5:c.314-15040T>G | ENSP00000437623.1:n.314-15040T>G | |
| ENST00000541189.5:c.339-15040T>G | ||
| ENST00000541897.5:c.*119-15040T>G | ENSP00000445051.1:n.*119-15040T>G | |
| ENST00000614640.4:c.293-15040T>G | ENSP00000481483.1:n.293-15040T>G | |
| NM_001031679.2:c.293-15040T>G | NP_001026849.1:n.293-15040T>G | |
| NM_001193460.1:c.293-15040T>G | NP_001180389.1:n.293-15040T>G | |
| NM_001193461.1:c.293-15040T>G | NP_001180390.1:n.293-15040T>G | |
| NM_198080.3:c.314-15040T>G | NP_932346.1:n.314-15040T>G | |
| XM_024448918.1:c.293-15040T>G | XP_024304686.1:n.293-15040T>G | |
| XM_024448919.1:c.293-15040T>G | XP_024304687.1:n.293-15040T>G | |
| XM_024448920.1:c.293-15040T>G | XP_024304688.1:n.293-15040T>G | |
| XM_024448921.1:c.293-15040T>G | XP_024304689.1:n.293-15040T>G | |
| NM_001031679.3:c.293-15040T>G MANE Select | NP_001026849.1:n.293-15040T>G | |
| NM_001193460.2:c.293-15040T>G | NP_001180389.1:n.293-15040T>G | |
| NM_198080.4:c.314-15040T>G | NP_932346.1:n.314-15040T>G | |
| NM_001193461.2:c.293-15040T>G | NP_001180390.1:n.293-15040T>G |