Linked Data
dbSNP Id:
rs763599698
gnomAD v2:
1-5923995-G-T
gnomAD v4:
1-5863935-G-T
COSMIC:
COSM4637737
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.5863935G>T , CM000663.2:g.5863935G>T | GRCh38 |
| NC_000001.10:g.5923995G>T , CM000663.1:g.5923995G>T | GRCh37 |
| NC_000001.9:g.5846582G>T | NCBI36 |
| NG_011724.2:g.133537C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378156.9:c.4095C>A MANE Select | ENSP00000367398.4:p.His1365Gln | |
| ENST00000378156.8:c.4095C>A | ENSP00000367398.4:p.His1365Gln | |
| ENST00000378161.5:n.3246C>A | ||
| ENST00000378169.7:c.*2996C>A | ENSP00000367411.3:n.*2996C>A | |
| ENST00000460696.1:n.2843C>A | ||
| ENST00000478423.6:n.3827C>A | ||
| ENST00000489180.6:c.*1906C>A | ENSP00000423747.1:n.*1906C>A | |
| NM_001291593.1:c.2556C>A | NP_001278522.1:p.His852Gln | |
| NM_001291594.1:c.2559C>A | NP_001278523.1:p.His853Gln | |
| NM_015102.4:c.4095C>A | NP_055917.1:p.His1365Gln | |
| NR_111987.1:n.4910C>A | ||
| XM_006710563.2:c.4095C>A | XP_006710626.1:p.His1365Gln | |
| XM_006710565.2:c.4095C>A | XP_006710628.1:p.His1365Gln | |
| XM_011541213.1:c.4092C>A | XP_011539515.1:p.His1364Gln | |
| XM_011541214.1:c.4053C>A | XP_011539516.1:p.His1351Gln | |
| XM_011541215.1:c.3984C>A | XP_011539517.1:p.His1328Gln | |
| XM_011541216.1:c.4095C>A | XP_011539518.1:p.His1365Gln | |
| XM_011541217.1:c.4095C>A | XP_011539519.1:p.His1365Gln | |
| XM_011541218.1:c.4095C>A | XP_011539520.1:p.His1365Gln | |
| XM_011541219.1:c.4041C>A | XP_011539521.1:p.His1347Gln | |
| XM_006710563.3:c.4095C>A | XP_006710626.1:p.His1365Gln | |
| XM_011541216.2:c.4095C>A | XP_011539518.1:p.His1365Gln | |
| XM_011541217.2:c.4095C>A | XP_011539519.1:p.His1365Gln | |
| XM_011541218.2:c.4095C>A | XP_011539520.1:p.His1365Gln | |
| XM_017000996.1:c.4050C>A | XP_016856485.1:p.His1350Gln | |
| XM_017000997.1:c.4095C>A | XP_016856486.1:p.His1365Gln | |
| XM_017000999.1:c.3567C>A | XP_016856488.1:p.His1189Gln | |
| XM_017001000.2:c.3567C>A | XP_016856489.1:p.His1189Gln | |
| XM_017001001.1:c.3297C>A | XP_016856490.1:p.His1099Gln | |
| XM_017001003.1:c.2556C>A | XP_016856492.1:p.His852Gln | |
| XR_001737114.1:n.3961C>A | ||
| XR_001737115.1:n.3946C>A | ||
| NM_015102.5:c.4095C>A MANE Select | NP_055917.1:p.His1365Gln | |
| NM_001291593.2:c.2556C>A | NP_001278522.1:p.His852Gln | |
| NM_001291594.2:c.2559C>A | NP_001278523.1:p.His853Gln | |
| NR_111987.2:n.4862C>A |