Linked Data
ClinVar Variation Id:
2040731
ClinVar RCV Id:
RCV002912682
MyVariant Identifiers:
chr3:g.189526297C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.189808508C>G , CM000665.2:g.189808508C>G | GRCh38 |
| NC_000003.11:g.189526297C>G , CM000665.1:g.189526297C>G | GRCh37 |
| NC_000003.10:g.191008991C>G | NCBI36 |
| NG_007550.1:g.182082C>G | |
| NG_007550.2:g.182082C>G | |
| NG_007550.3:g.216763C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264731.8:c.561C>G MANE Select | ENSP00000264731.3:p.Ala187= | |
| ENST00000354600.10:c.279C>G MANE Plus Clinical | ENSP00000346614.5:p.Ala93= | |
| ENST00000264731.7:c.561C>G | ENSP00000264731.3:p.Ala187= | |
| ENST00000320472.9:c.561C>G | ENSP00000317510.5:p.Ala187= | |
| ENST00000354600.9:c.279C>G | ENSP00000346614.5:p.Ala93= | |
| ENST00000392460.7:c.561C>G | ENSP00000376253.3:p.Ala187= | |
| ENST00000392461.7:c.279C>G | ENSP00000376254.3:p.Ala93= | |
| ENST00000392463.6:c.279C>G | ENSP00000376256.2:p.Ala93= | |
| ENST00000418709.6:c.561C>G | ENSP00000407144.2:p.Ala187= | |
| ENST00000434928.5:c.279C>G | ENSP00000401661.1:p.Ala93= | |
| ENST00000437221.5:c.279C>G | ENSP00000392488.1:p.Ala93= | |
| ENST00000440651.6:c.561C>G | ENSP00000394337.2:p.Ala187= | |
| ENST00000449992.5:c.42+18666C>G | ENSP00000387839.1:n.42+18666C>G | |
| ENST00000456148.1:c.279C>G | ENSP00000389485.1:p.Ala93= | |
| ENST00000460036.1:n.385C>G | ||
| NM_001114978.1:c.561C>G | NP_001108450.1:p.Ala187= | |
| NM_001114979.1:c.561C>G | NP_001108451.1:p.Ala187= | |
| NM_001114980.1:c.279C>G | NP_001108452.1:p.Ala93= | |
| NM_001114981.1:c.279C>G | NP_001108453.1:p.Ala93= | |
| NM_001114982.1:c.279C>G | NP_001108454.1:p.Ala93= | |
| NM_003722.4:c.561C>G | NP_003713.3:p.Ala187= | |
| XM_005247843.2:c.561C>G | XP_005247900.1:p.Ala187= | |
| XM_005247844.3:c.510C>G | XP_005247901.1:p.Ala170= | |
| XM_005247846.2:c.561C>G | XP_005247903.1:p.Ala187= | |
| XM_011513251.1:c.558C>G | XP_011511553.1:p.Ala186= | |
| XM_011513252.1:c.555C>G | XP_011511554.1:p.Ala185= | |
| XM_011513253.1:c.522C>G | XP_011511555.1:p.Ala174= | |
| NM_001329144.1:c.561C>G | NP_001316073.1:p.Ala187= | |
| NM_001329145.1:c.279C>G | NP_001316074.1:p.Ala93= | |
| NM_001329146.1:c.42+18666C>G | NP_001316075.1:n.42+18666C>G | |
| NM_001329148.1:c.561C>G | NP_001316077.1:p.Ala187= | |
| NM_001329149.1:c.279C>G | NP_001316078.1:p.Ala93= | |
| NM_001329150.1:c.42+18666C>G | NP_001316079.1:n.42+18666C>G | |
| NM_001329964.1:c.555C>G | NP_001316893.1:p.Ala185= | |
| NM_003722.5:c.561C>G MANE Select | NP_003713.3:p.Ala187= | |
| NM_001114978.2:c.561C>G | NP_001108450.1:p.Ala187= | |
| NM_001114979.2:c.561C>G | NP_001108451.1:p.Ala187= | |
| NM_001114980.2:c.279C>G MANE Plus Clinical | NP_001108452.1:p.Ala93= | |
| NM_001114981.2:c.279C>G | NP_001108453.1:p.Ala93= | |
| NM_001114982.2:c.279C>G | NP_001108454.1:p.Ala93= | |
| NM_001329144.2:c.561C>G | NP_001316073.1:p.Ala187= | |
| NM_001329145.2:c.279C>G | NP_001316074.1:p.Ala93= | |
| NM_001329146.2:c.42+18666C>G | NP_001316075.1:n.42+18666C>G | |
| NM_001329148.2:c.561C>G | NP_001316077.1:p.Ala187= | |
| NM_001329149.2:c.279C>G | NP_001316078.1:p.Ala93= | |
| NM_001329150.2:c.42+18666C>G | NP_001316079.1:n.42+18666C>G | |
| NM_001329964.2:c.555C>G | NP_001316893.1:p.Ala185= |