Linked Data
ClinVar Variation Id:
2697949
ClinVar RCV Id:
RCV003551521
gnomAD v4:
8-6455195-C-G
MyVariant Identifiers:
chr8:g.6312716C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.6455195C>G , CM000670.2:g.6455195C>G | GRCh38 |
| NC_000008.10:g.6312716C>G , CM000670.1:g.6312716C>G | GRCh37 |
| NC_000008.9:g.6300124C>G | NCBI36 |
| NG_016619.1:g.53604C>G | |
| NG_016619.2:g.53604C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000687720.1:c.*1826C>G | ENSP00000510728.1:n.*1826C>G | |
| ENST00000687874.1:n.738C>G | ||
| ENST00000688101.1:c.1298C>G | ||
| ENST00000688388.1:c.1878C>G | ENSP00000510092.1:p.Gly626= | |
| ENST00000688658.1:n.718C>G | ||
| ENST00000688912.1:n.1889C>G | ||
| ENST00000689348.1:c.1878C>G | ENSP00000509554.1:p.Gly626= | |
| ENST00000689633.1:c.1878C>G | ENSP00000509054.1:p.Gly626= | |
| ENST00000689736.1:c.723C>G | ENSP00000509722.1:p.Gly241= | |
| ENST00000690159.1:c.*2157C>G | ENSP00000510482.1:n.*2157C>G | |
| ENST00000690708.1:c.723C>G | ENSP00000510400.1:p.Gly241= | |
| ENST00000690826.1:c.1878C>G | ENSP00000510536.1:p.Gly626= | |
| ENST00000691435.1:c.1878C>G | ENSP00000510652.1:p.Gly626= | |
| ENST00000691655.1:c.*733C>G | ENSP00000509652.1:n.*733C>G | |
| ENST00000692534.1:c.256C>G | ||
| ENST00000692836.1:c.1878C>G | ENSP00000509971.1:p.Gly626= | |
| ENST00000692938.1:c.1878C>G | ENSP00000509072.1:p.Gly626= | |
| ENST00000693231.1:c.*1618C>G | ENSP00000510764.1:n.*1618C>G | |
| ENST00000693528.1:n.111C>G | ||
| ENST00000344683.10:c.1878C>G MANE Select | ENSP00000342924.5:p.Gly626= | |
| ENST00000344683.9:c.1878C>G | ENSP00000342924.5:p.Gly626= | |
| NM_024596.3:c.1878C>G | NP_078872.2:p.Gly626= | |
| XM_011534755.1:c.1878C>G | XP_011533057.1:p.Gly626= | |
| XM_011534756.1:c.1878C>G | XP_011533058.1:p.Gly626= | |
| XM_011534757.1:c.1878C>G | XP_011533059.1:p.Gly626= | |
| XM_011534758.1:c.1878C>G | XP_011533060.1:p.Gly626= | |
| XM_011534759.1:c.1878C>G | XP_011533061.1:p.Gly626= | |
| XM_011534760.1:c.1353C>G | XP_011533062.1:p.Gly451= | |
| NM_001322042.1:c.1878C>G | NP_001308971.1:p.Gly626= | |
| NM_001363979.1:c.1878C>G | NP_001350908.1:p.Gly626= | |
| NM_001363980.1:c.1878C>G | NP_001350909.1:p.Gly626= | |
| NM_024596.4:c.1878C>G | NP_078872.2:p.Gly626= | |
| XM_011534755.3:c.1878C>G | XP_011533057.1:p.Gly626= | |
| XM_011534756.3:c.1878C>G | XP_011533058.1:p.Gly626= | |
| XM_011534757.3:c.1878C>G | XP_011533059.1:p.Gly626= | |
| XM_011534758.3:c.1878C>G | XP_011533060.1:p.Gly626= | |
| XM_011534759.3:c.1878C>G | XP_011533061.1:p.Gly626= | |
| XM_011534760.2:c.1353C>G | XP_011533062.1:p.Gly451= | |
| XM_017013829.2:c.1878C>G | XP_016869318.1:p.Gly626= | |
| XM_017013831.2:c.1878C>G | XP_016869320.1:p.Gly626= | |
| XM_017013832.2:c.1878C>G | XP_016869321.1:p.Gly626= | |
| XM_017013833.2:c.1878C>G | XP_016869322.1:p.Gly626= | |
| XR_001745596.2:n.1931C>G | ||
| NM_024596.5:c.1878C>G MANE Select | NP_078872.3:p.Gly626= | |
| NM_001322042.2:c.1878C>G | NP_001308971.2:p.Gly626= | |
| NM_001363980.2:c.1878C>G | NP_001350909.1:p.Gly626= |