Linked Data
ClinVar Variation Id:
1956022
ClinVar RCV Id:
RCV002700524
MyVariant Identifiers:
chr12:g.48377517T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.47983734T>A , CM000674.2:g.47983734T>A | GRCh38 |
| NC_000012.11:g.48377517T>A , CM000674.1:g.48377517T>A | GRCh37 |
| NC_000012.10:g.46663784T>A | NCBI36 |
| NG_008072.1:g.25769A>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000337299.7:c.1737A>T | ENSP00000338213.6:p.Gly579= | |
| ENST00000380518.8:c.1944A>T MANE Select | ENSP00000369889.3:p.Gly648= | |
| ENST00000337299.6:c.1737A>T | ENSP00000338213.6:p.Gly579= | |
| ENST00000380518.7:c.1944A>T | ENSP00000369889.3:p.Gly648= | |
| ENST00000483376.1:n.122A>T | ||
| ENST00000493991.5:n.868A>T | ||
| NM_001844.4:c.1944A>T | NP_001835.3:p.Gly648= | |
| NM_033150.2:c.1737A>T | NP_149162.2:p.Gly579= | |
| XM_006719242.2:c.2088A>T | XP_006719305.2:p.Gly696= | |
| XM_011537928.1:c.2088A>T | XP_011536230.1:p.Gly696= | |
| XM_011537929.1:c.2088A>T | XP_011536231.1:p.Gly696= | |
| XM_011537930.1:c.2088A>T | XP_011536232.1:p.Gly696= | |
| XM_011537931.1:c.2088A>T | XP_011536233.1:p.Gly696= | |
| XM_011537932.1:c.2088A>T | XP_011536234.1:p.Gly696= | |
| XM_011537933.1:c.2088A>T | XP_011536235.1:p.Gly696= | |
| XM_011537934.1:c.2085A>T | XP_011536236.1:p.Gly695= | |
| XM_011537935.1:c.1032A>T | XP_011536237.1:p.Gly344= | |
| XM_017018828.1:c.2088A>T | XP_016874317.1:p.Gly696= | |
| XM_017018829.1:c.2085A>T | XP_016874318.1:p.Gly695= | |
| XM_017018830.1:c.1878A>T | XP_016874319.1:p.Gly626= | |
| XM_017018831.2:c.1398A>T | XP_016874320.1:p.Gly466= | |
| NM_001844.5:c.1944A>T MANE Select | NP_001835.3:p.Gly648= | |
| NM_033150.3:c.1737A>T | NP_149162.2:p.Gly579= |