Linked Data
ClinVar Variation Id:
246280
dbSNP Id:
rs62621089
ExAC:
19:10286289 G / A
gnomAD v2:
19-10286289-G-A
gnomAD v3:
19-10175613-G-A
gnomAD v4:
19-10175613-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.10175613G>A , CM000681.2:g.10175613G>A | GRCh38 |
| NC_000019.9:g.10286289G>A , CM000681.1:g.10286289G>A | GRCh37 |
| NC_000019.8:g.10147289G>A | NCBI36 |
| NG_028016.3:g.60674C>T , LRG_362:g.60674C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000359526.9:c.575C>T MANE Select | ENSP00000352516.3:p.Ala192Val | |
| ENST00000676604.1:n.181C>T | ||
| ENST00000676610.1:c.527C>T | ENSP00000504236.1:p.Ala176Val | |
| ENST00000676820.1:n.583C>T | ||
| ENST00000677013.1:c.*217C>T | ENSP00000503135.1:n.*217C>T | |
| ENST00000677250.1:c.527C>T | ENSP00000502894.1:p.Ala176Val | |
| ENST00000677616.1:c.212C>T | ENSP00000503055.1:p.Ala71Val | |
| ENST00000677634.1:c.527C>T | ENSP00000504246.1:p.Ala176Val | |
| ENST00000677685.1:c.307C>T | ENSP00000503407.1:p.Pro103Ser | |
| ENST00000677946.1:c.527C>T | ENSP00000504202.1:p.Ala176Val | |
| ENST00000678024.1:n.664C>T | ||
| ENST00000678804.1:c.527C>T | ENSP00000503853.1:p.Ala176Val | |
| ENST00000679103.1:c.527C>T | ENSP00000503151.1:p.Ala176Val | |
| ENST00000679313.1:c.527C>T | ENSP00000504512.1:p.Ala176Val | |
| ENST00000340748.8:c.527C>T | ENSP00000345739.3:p.Ala176Val | |
| ENST00000359526.8:c.575C>T | ENSP00000352516.3:p.Ala192Val | |
| ENST00000540357.5:c.-482C>T | ENSP00000440457.2:n.-482C>T | |
| ENST00000586988.5:c.*355C>T | ENSP00000464958.1:n.*355C>T | |
| ENST00000588118.5:c.692C>T | ENSP00000465223.1:p.Ala231Val | |
| ENST00000588952.5:c.164C>T | ENSP00000467050.1:p.Ala55Val | |
| ENST00000592054.5:c.164C>T | ENSP00000468359.1:p.Ala55Val | |
| ENST00000592342.5:c.212C>T | ENSP00000465993.1:p.Ala71Val | |
| ENST00000592705.5:c.*265C>T | ENSP00000466657.1:n.*265C>T | |
| NM_001130823.1:c.575C>T , LRG_362t1:c.575C>T | NP_001124295.1:p.Ala192Val | |
| NM_001379.2:c.527C>T | NP_001370.1:p.Ala176Val | |
| XM_011527772.1:c.575C>T | XP_011526074.1:p.Ala192Val | |
| XM_011527773.1:c.527C>T | XP_011526075.1:p.Ala176Val | |
| XM_011527774.1:c.164C>T | XP_011526076.1:p.Ala55Val | |
| NM_001130823.2:c.575C>T | NP_001124295.1:p.Ala192Val | |
| NM_001318730.1:c.527C>T | NP_001305659.1:p.Ala176Val | |
| NM_001318731.1:c.212C>T | NP_001305660.1:p.Ala71Val | |
| NM_001379.3:c.527C>T | NP_001370.1:p.Ala176Val | |
| NM_001130823.3:c.575C>T MANE Select | NP_001124295.1:p.Ala192Val | |
| NM_001318730.2:c.527C>T | NP_001305659.1:p.Ala176Val | |
| NM_001318731.2:c.212C>T | NP_001305660.1:p.Ala71Val | |
| NM_001379.4:c.527C>T | NP_001370.1:p.Ala176Val |