Linked Data
ClinVar Variation Id:
1412322
ClinVar RCV Id:
RCV001919066
dbSNP Id:
rs978921089
gnomAD v2:
12-48371188-G-A
gnomAD v4:
12-47977405-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.47977405G>A , CM000674.2:g.47977405G>A | GRCh38 |
| NC_000012.11:g.48371188G>A , CM000674.1:g.48371188G>A | GRCh37 |
| NC_000012.10:g.46657455G>A | NCBI36 |
| NG_008072.1:g.32098C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000337299.7:c.2981C>T | ENSP00000338213.6:p.Ala994Val | |
| ENST00000380518.8:c.3188C>T MANE Select | ENSP00000369889.3:p.Ala1063Val | |
| ENST00000337299.6:c.2981C>T | ENSP00000338213.6:p.Ala994Val | |
| ENST00000380518.7:c.3188C>T | ENSP00000369889.3:p.Ala1063Val | |
| ENST00000493991.5:n.2274C>T | ||
| ENST00000546974.1:n.41C>T | ||
| NM_001844.4:c.3188C>T | NP_001835.3:p.Ala1063Val | |
| NM_033150.2:c.2981C>T | NP_149162.2:p.Ala994Val | |
| XM_006719242.2:c.3332C>T | XP_006719305.2:p.Ala1111Val | |
| XM_011537928.1:c.3332C>T | XP_011536230.1:p.Ala1111Val | |
| XM_011537929.1:c.3332C>T | XP_011536231.1:p.Ala1111Val | |
| XM_011537930.1:c.3332C>T | XP_011536232.1:p.Ala1111Val | |
| XM_011537931.1:c.3332C>T | XP_011536233.1:p.Ala1111Val | |
| XM_011537932.1:c.3332C>T | XP_011536234.1:p.Ala1111Val | |
| XM_011537933.1:c.3332C>T | XP_011536235.1:p.Ala1111Val | |
| XM_011537934.1:c.3329C>T | XP_011536236.1:p.Ala1110Val | |
| XM_011537935.1:c.2276C>T | XP_011536237.1:p.Ala759Val | |
| XM_017018828.1:c.3332C>T | XP_016874317.1:p.Ala1111Val | |
| XM_017018829.1:c.3329C>T | XP_016874318.1:p.Ala1110Val | |
| XM_017018830.1:c.3122C>T | XP_016874319.1:p.Ala1041Val | |
| XM_017018831.2:c.2642C>T | XP_016874320.1:p.Ala881Val | |
| NM_001844.5:c.3188C>T MANE Select | NP_001835.3:p.Ala1063Val | |
| NM_033150.3:c.2981C>T | NP_149162.2:p.Ala994Val |