Linked Data
dbSNP Id:
rs758185308
ExAC:
20:13782217 A / G
gnomAD v2:
20-13782217-A-G
gnomAD v4:
20-13801571-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.13801571A>G , CM000682.2:g.13801571A>G | GRCh38 |
| NC_000020.10:g.13782217A>G , CM000682.1:g.13782217A>G | GRCh37 |
| NC_000020.9:g.13730217A>G | NCBI36 |
| NG_015811.1:g.21546A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378106.10:c.605A>G MANE Select | ENSP00000367346.5:p.Gln202Arg | |
| ENST00000378081.9:c.605A>G | ENSP00000437325.1:p.Gln202Arg | |
| ENST00000378106.9:c.605A>G | ENSP00000367346.5:p.Gln202Arg | |
| ENST00000463598.1:c.521A>G | ENSP00000420497.1:p.Gln174Arg | |
| ENST00000464269.5:n.278A>G | ||
| ENST00000475968.5:n.482A>G | ||
| ENST00000476124.1:n.4A>G | ||
| ENST00000476536.5:n.565A>G | ||
| ENST00000477732.5:n.502+3071A>G | ||
| ENST00000479716.5:n.126A>G | ||
| ENST00000481249.5:n.482A>G | ||
| ENST00000485738.5:n.582A>G | ||
| ENST00000487478.5:n.29A>G | ||
| NM_001039375.2:c.521A>G | NP_001034464.1:p.Gln174Arg | |
| NM_024120.4:c.605A>G | NP_077025.2:p.Gln202Arg | |
| NR_029377.1:n.648A>G | ||
| XM_006723620.2:c.605A>G | XP_006723683.1:p.Gln202Arg | |
| XM_006723622.2:c.134A>G | XP_006723685.1:p.Gln45Arg | |
| XM_006723623.1:c.134A>G | XP_006723686.1:p.Gln45Arg | |
| XM_006723624.1:c.134A>G | XP_006723687.1:p.Gln45Arg | |
| XM_011529341.1:c.605A>G | XP_011527643.1:p.Gln202Arg | |
| XM_011529342.1:c.605A>G | XP_011527644.1:p.Gln202Arg | |
| XM_011529343.1:c.605A>G | XP_011527645.1:p.Gln202Arg | |
| XM_011529344.1:c.236A>G | XP_011527646.1:p.Gln79Arg | |
| XR_430269.2:n.625A>G | ||
| XR_937140.1:n.625A>G | ||
| NM_001352403.1:c.134A>G | NP_001339332.1:p.Gln45Arg | |
| NM_001352406.1:c.44A>G | NP_001339335.1:p.Gln15Arg | |
| NM_001352407.1:c.44A>G | NP_001339336.1:p.Gln15Arg | |
| NM_001352408.1:c.605A>G | NP_001339337.1:p.Gln202Arg | |
| NR_147978.1:n.648A>G | ||
| NR_147979.1:n.668A>G | ||
| NR_147980.1:n.544A>G | ||
| NR_147981.1:n.782A>G | ||
| NR_147982.1:n.782A>G | ||
| NR_147983.1:n.698A>G | ||
| XM_006723624.2:c.134A>G | XP_006723687.1:p.Gln45Arg | |
| XM_011529342.2:c.605A>G | XP_011527644.1:p.Gln202Arg | |
| XM_024451999.1:c.134A>G | XP_024307767.1:p.Gln45Arg | |
| XR_001754396.1:n.564A>G | ||
| XR_430269.3:n.625A>G | ||
| XR_937140.2:n.625A>G | ||
| NM_024120.5:c.605A>G MANE Select | NP_077025.2:p.Gln202Arg | |
| NM_001039375.3:c.521A>G | NP_001034464.1:p.Gln174Arg | |
| NM_001352403.2:c.134A>G | NP_001339332.1:p.Gln45Arg | |
| NM_001352406.2:c.44A>G | NP_001339335.1:p.Gln15Arg | |
| NM_001352407.2:c.44A>G | NP_001339336.1:p.Gln15Arg | |
| NR_029377.2:n.646A>G | ||
| NR_147978.2:n.646A>G | ||
| NR_147979.2:n.666A>G | ||
| NR_147980.2:n.542A>G | ||
| NR_147981.2:n.780A>G | ||
| NR_147982.2:n.780A>G | ||
| NR_147983.2:n.696A>G | ||
| NM_001352408.2:c.605A>G | NP_001339337.1:p.Gln202Arg |