Linked Data
ClinVar Variation Id:
1544052
ClinVar RCV Id:
RCV002172693
dbSNP Id:
rs372837897
ExAC:
11:118897337 G / A
gnomAD v2:
11-118897337-G-A
gnomAD v3:
11-119026627-G-A
gnomAD v4:
11-119026627-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.119026627G>A , CM000673.2:g.119026627G>A | GRCh38 |
| NC_000011.9:g.118897337G>A , CM000673.1:g.118897337G>A | GRCh37 |
| NC_000011.8:g.118402547G>A | NCBI36 |
| NG_013331.1:g.9279C>T , LRG_187:g.9279C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000529510.6:n.1014+310C>T | ||
| ENST00000697845.1:n.1248C>T | ||
| ENST00000697846.1:n.1014+310C>T | ||
| ENST00000697847.1:n.1076C>T | ||
| ENST00000697848.1:n.1076C>T | ||
| ENST00000697849.1:n.2363C>T | ||
| ENST00000697850.1:n.1076C>T | ||
| ENST00000697851.1:n.2684C>T | ||
| ENST00000638186.1:n.1150C>T | ||
| ENST00000638360.1:n.982C>T | ||
| ENST00000638925.1:n.1083C>T | ||
| ENST00000650539.1:n.1252C>T | ||
| ENST00000330775.9:c.846C>T | ENSP00000476242.2:p.Tyr282= | |
| ENST00000357590.9:c.846C>T | ENSP00000476176.2:p.Tyr282= | |
| ENST00000524428.5:n.1106+310C>T | ||
| ENST00000525039.5:n.1270C>T | ||
| ENST00000525102.5:n.1604C>T | ||
| ENST00000525372.5:n.847C>T | ||
| ENST00000526275.5:n.1628C>T | ||
| ENST00000527992.5:n.1074C>T | ||
| ENST00000529510.5:n.558+310C>T | ||
| ENST00000530407.5:n.996C>T | ||
| ENST00000532085.1:n.3705C>T | ||
| ENST00000538950.5:c.627C>T | ENSP00000475991.2:p.Tyr209= | |
| ENST00000545985.5:c.846C>T | ENSP00000475241.2:p.Tyr282= | |
| NM_001164277.1:c.846C>T , LRG_187t1:c.846C>T | NP_001157749.1:p.Tyr282= | |
| NM_001164278.1:c.846C>T | NP_001157750.1:p.Tyr282= | |
| NM_001164279.1:c.627C>T | NP_001157751.1:p.Tyr209= | |
| NM_001164280.1:c.846C>T | NP_001157752.1:p.Tyr282= | |
| NM_001467.5:c.846C>T | NP_001458.1:p.Tyr282= | |
| NM_001164278.2:c.846C>T | NP_001157750.1:p.Tyr282= | |
| NM_001164279.2:c.627C>T | NP_001157751.1:p.Tyr209= | |
| NM_001164280.2:c.846C>T | NP_001157752.1:p.Tyr282= | |
| NM_001467.6:c.846C>T | NP_001458.1:p.Tyr282= | |
| NM_001164277.2:c.846C>T MANE Select | NP_001157749.1:p.Tyr282= |