Linked Data
ClinVar Variation Id:
1015644
ClinVar RCV Id:
RCV001314530
dbSNP Id:
rs1554669404
gnomAD v4:
8-143916514-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.143916514G>C , CM000670.2:g.143916514G>C | GRCh38 |
| NC_000008.10:g.144990682G>C , CM000670.1:g.144990682G>C | GRCh37 |
| NC_000008.9:g.145062670G>C | NCBI36 |
| NG_012492.1:g.65232C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000528025.6:c.13439C>G | ENSP00000437303.2:p.Thr4480Ser | |
| ENST00000685198.1:c.13358C>G | ENSP00000510528.1:p.Thr4453Ser | |
| ENST00000687971.1:c.13025C>G | ENSP00000510788.1:p.Thr4342Ser | |
| ENST00000693060.1:c.13238C>G | ENSP00000510329.1:p.Thr4413Ser | |
| ENST00000345136.8:c.13307C>G MANE Select | ENSP00000344848.3:p.Thr4436Ser | |
| ENST00000527303.2:c.10007C>G | ENSP00000433982.2:p.Thr3336Ser | |
| ENST00000322810.8:c.13718C>G | ENSP00000323856.4:p.Thr4573Ser | |
| ENST00000345136.7:c.13307C>G | ENSP00000344848.3:p.Thr4436Ser | |
| ENST00000354589.7:c.13307C>G | ENSP00000346602.3:p.Thr4436Ser | |
| ENST00000354958.6:c.13241C>G | ENSP00000347044.2:p.Thr4414Ser | |
| ENST00000356346.7:c.13265C>G MANE Plus Clinical | ENSP00000348702.3:p.Thr4422Ser | |
| ENST00000357649.6:c.13319C>G | ENSP00000350277.2:p.Thr4440Ser | |
| ENST00000398774.6:c.13211C>G | ENSP00000381756.2:p.Thr4404Ser | |
| ENST00000436759.6:c.13388C>G | ENSP00000388180.2:p.Thr4463Ser | |
| ENST00000527096.5:c.13376C>G | ENSP00000434583.1:p.Thr4459Ser | |
| NM_000445.4:c.13388C>G | NP_000436.2:p.Thr4463Ser | |
| NM_201378.3:c.13265C>G | NP_958780.1:p.Thr4422Ser | |
| NM_201379.2:c.13241C>G | NP_958781.1:p.Thr4414Ser | |
| NM_201380.3:c.13718C>G | NP_958782.1:p.Thr4573Ser | |
| NM_201381.2:c.13211C>G | NP_958783.1:p.Thr4404Ser | |
| NM_201382.3:c.13307C>G | NP_958784.1:p.Thr4436Ser | |
| NM_201383.2:c.13319C>G | NP_958785.1:p.Thr4440Ser | |
| NM_201384.2:c.13307C>G | NP_958786.1:p.Thr4436Ser | |
| XM_005250976.2:c.13733C>G | XP_005251033.1:p.Thr4578Ser | |
| XM_005250978.2:c.13334C>G | XP_005251035.1:p.Thr4445Ser | |
| XM_005250979.3:c.13322C>G | XP_005251036.1:p.Thr4441Ser | |
| XM_005250980.3:c.13322C>G | XP_005251037.1:p.Thr4441Ser | |
| XM_005250981.2:c.13280C>G | XP_005251038.1:p.Thr4427Ser | |
| XM_005250982.2:c.13256C>G | XP_005251039.1:p.Thr4419Ser | |
| XM_005250983.2:c.13238C>G | XP_005251040.1:p.Thr4413Ser | |
| XM_005250984.3:c.13226C>G | XP_005251041.1:p.Thr4409Ser | |
| XM_006716588.2:c.13403C>G | XP_006716651.1:p.Thr4468Ser | |
| XM_006716589.2:c.13253C>G | XP_006716652.1:p.Thr4418Ser | |
| XM_006716590.2:c.13253C>G | XP_006716653.1:p.Thr4418Ser | |
| XM_011517130.1:c.13322C>G | XP_011515432.1:p.Thr4441Ser | |
| XM_011517131.1:c.13238C>G | XP_011515433.1:p.Thr4413Ser | |
| XM_011517132.1:c.9953C>G | XP_011515434.1:p.Thr3318Ser | |
| XM_005250976.4:c.13733C>G | XP_005251033.1:p.Thr4578Ser | |
| XM_005250978.3:c.13334C>G | XP_005251035.1:p.Thr4445Ser | |
| XM_005250979.4:c.13322C>G | XP_005251036.1:p.Thr4441Ser | |
| XM_005250980.4:c.13322C>G | XP_005251037.1:p.Thr4441Ser | |
| XM_005250981.3:c.13280C>G | XP_005251038.1:p.Thr4427Ser | |
| XM_005250982.4:c.13256C>G | XP_005251039.1:p.Thr4419Ser | |
| XM_005250984.5:c.13226C>G | XP_005251041.1:p.Thr4409Ser | |
| XM_006716588.3:c.13403C>G | XP_006716651.1:p.Thr4468Ser | |
| XM_006716590.3:c.13253C>G | XP_006716653.1:p.Thr4418Ser | |
| XM_011517130.2:c.13322C>G | XP_011515432.1:p.Thr4441Ser | |
| XM_011517131.2:c.13238C>G | XP_011515433.1:p.Thr4413Ser | |
| XM_011517132.2:c.9953C>G | XP_011515434.1:p.Thr3318Ser | |
| NM_000445.5:c.13388C>G | NP_000436.2:p.Thr4463Ser | |
| NM_201378.4:c.13265C>G MANE Plus Clinical | NP_958780.1:p.Thr4422Ser | |
| NM_201379.3:c.13241C>G | NP_958781.1:p.Thr4414Ser | |
| NM_201380.4:c.13718C>G | NP_958782.1:p.Thr4573Ser | |
| NM_201381.3:c.13211C>G | NP_958783.1:p.Thr4404Ser | |
| NM_201382.4:c.13307C>G | NP_958784.1:p.Thr4436Ser | |
| NM_201383.3:c.13319C>G | NP_958785.1:p.Thr4440Ser | |
| NM_201384.3:c.13307C>G MANE Select | NP_958786.1:p.Thr4436Ser |