Linked Data
ClinVar Variation Id:
498962
dbSNP Id:
rs782370134
gnomAD v2:
8-144995316-G-C
gnomAD v3:
8-143921148-G-C
gnomAD v4:
8-143921148-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.143921148G>C , CM000670.2:g.143921148G>C | GRCh38 |
| NC_000008.10:g.144995316G>C , CM000670.1:g.144995316G>C | GRCh37 |
| NC_000008.9:g.145067304G>C | NCBI36 |
| NG_012492.1:g.60598C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000528025.6:c.8805C>G | ENSP00000437303.2:p.Gly2935= | |
| ENST00000685198.1:c.8724C>G | ENSP00000510528.1:p.Gly2908= | |
| ENST00000687971.1:c.8391C>G | ENSP00000510788.1:p.Gly2797= | |
| ENST00000693060.1:c.8604C>G | ENSP00000510329.1:p.Gly2868= | |
| ENST00000345136.8:c.8673C>G MANE Select | ENSP00000344848.3:p.Gly2891= | |
| ENST00000527303.2:c.5373C>G | ENSP00000433982.2:p.Gly1791= | |
| ENST00000322810.8:c.9084C>G | ENSP00000323856.4:p.Gly3028= | |
| ENST00000345136.7:c.8673C>G | ENSP00000344848.3:p.Gly2891= | |
| ENST00000354589.7:c.8673C>G | ENSP00000346602.3:p.Gly2891= | |
| ENST00000354958.6:c.8607C>G | ENSP00000347044.2:p.Gly2869= | |
| ENST00000356346.7:c.8631C>G MANE Plus Clinical | ENSP00000348702.3:p.Gly2877= | |
| ENST00000357649.6:c.8685C>G | ENSP00000350277.2:p.Gly2895= | |
| ENST00000398774.6:c.8577C>G | ENSP00000381756.2:p.Gly2859= | |
| ENST00000436759.6:c.8754C>G | ENSP00000388180.2:p.Gly2918= | |
| ENST00000527096.5:c.8742C>G | ENSP00000434583.1:p.Gly2914= | |
| NM_000445.4:c.8754C>G | NP_000436.2:p.Gly2918= | |
| NM_201378.3:c.8631C>G | NP_958780.1:p.Gly2877= | |
| NM_201379.2:c.8607C>G | NP_958781.1:p.Gly2869= | |
| NM_201380.3:c.9084C>G | NP_958782.1:p.Gly3028= | |
| NM_201381.2:c.8577C>G | NP_958783.1:p.Gly2859= | |
| NM_201382.3:c.8673C>G | NP_958784.1:p.Gly2891= | |
| NM_201383.2:c.8685C>G | NP_958785.1:p.Gly2895= | |
| NM_201384.2:c.8673C>G | NP_958786.1:p.Gly2891= | |
| XM_005250976.2:c.9099C>G | XP_005251033.1:p.Gly3033= | |
| XM_005250978.2:c.8700C>G | XP_005251035.1:p.Gly2900= | |
| XM_005250979.3:c.8688C>G | XP_005251036.1:p.Gly2896= | |
| XM_005250980.3:c.8688C>G | XP_005251037.1:p.Gly2896= | |
| XM_005250981.2:c.8646C>G | XP_005251038.1:p.Gly2882= | |
| XM_005250982.2:c.8622C>G | XP_005251039.1:p.Gly2874= | |
| XM_005250983.2:c.8604C>G | XP_005251040.1:p.Gly2868= | |
| XM_005250984.3:c.8592C>G | XP_005251041.1:p.Gly2864= | |
| XM_006716588.2:c.8769C>G | XP_006716651.1:p.Gly2923= | |
| XM_006716589.2:c.8619C>G | XP_006716652.1:p.Gly2873= | |
| XM_006716590.2:c.8619C>G | XP_006716653.1:p.Gly2873= | |
| XM_011517130.1:c.8688C>G | XP_011515432.1:p.Gly2896= | |
| XM_011517131.1:c.8604C>G | XP_011515433.1:p.Gly2868= | |
| XM_011517132.1:c.5319C>G | XP_011515434.1:p.Gly1773= | |
| XM_005250976.4:c.9099C>G | XP_005251033.1:p.Gly3033= | |
| XM_005250978.3:c.8700C>G | XP_005251035.1:p.Gly2900= | |
| XM_005250979.4:c.8688C>G | XP_005251036.1:p.Gly2896= | |
| XM_005250980.4:c.8688C>G | XP_005251037.1:p.Gly2896= | |
| XM_005250981.3:c.8646C>G | XP_005251038.1:p.Gly2882= | |
| XM_005250982.4:c.8622C>G | XP_005251039.1:p.Gly2874= | |
| XM_005250984.5:c.8592C>G | XP_005251041.1:p.Gly2864= | |
| XM_006716588.3:c.8769C>G | XP_006716651.1:p.Gly2923= | |
| XM_006716590.3:c.8619C>G | XP_006716653.1:p.Gly2873= | |
| XM_011517130.2:c.8688C>G | XP_011515432.1:p.Gly2896= | |
| XM_011517131.2:c.8604C>G | XP_011515433.1:p.Gly2868= | |
| XM_011517132.2:c.5319C>G | XP_011515434.1:p.Gly1773= | |
| NM_000445.5:c.8754C>G | NP_000436.2:p.Gly2918= | |
| NM_201378.4:c.8631C>G MANE Plus Clinical | NP_958780.1:p.Gly2877= | |
| NM_201379.3:c.8607C>G | NP_958781.1:p.Gly2869= | |
| NM_201380.4:c.9084C>G | NP_958782.1:p.Gly3028= | |
| NM_201381.3:c.8577C>G | NP_958783.1:p.Gly2859= | |
| NM_201382.4:c.8673C>G | NP_958784.1:p.Gly2891= | |
| NM_201383.3:c.8685C>G | NP_958785.1:p.Gly2895= | |
| NM_201384.3:c.8673C>G MANE Select | NP_958786.1:p.Gly2891= |