Linked Data
ClinVar Variation Id:
407123
ClinVar RCV Id:
RCV002365628
dbSNP Id:
rs370652082
ExAC:
9:130588029 C / T
gnomAD v2:
9-130588029-C-T
gnomAD v3:
9-127825750-C-T
gnomAD v4:
9-127825750-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.127825750C>T , CM000671.2:g.127825750C>T | GRCh38 |
| NC_000009.11:g.130588029C>T , CM000671.1:g.130588029C>T | GRCh37 |
| NC_000009.10:g.129627850C>T | NCBI36 |
| NG_009551.1:g.34019G>A , LRG_589:g.34019G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000480266.6:c.88G>A | ENSP00000479015.1:p.Val30Met | |
| ENST00000373203.9:c.634G>A MANE Select | ENSP00000362299.4:p.Val212Met | |
| ENST00000344849.4:c.634G>A | ENSP00000341917.3:p.Val212Met | |
| ENST00000373203.8:c.634G>A | ENSP00000362299.4:p.Val212Met | |
| ENST00000480266.5:c.88G>A | ENSP00000479015.1:p.Val30Met | |
| NM_000118.3:c.634G>A , LRG_589t1:c.634G>A | NP_000109.1:p.Val212Met | |
| NM_001114753.2:c.634G>A , LRG_589t2:c.634G>A | NP_001108225.1:p.Val212Met | |
| NM_001278138.1:c.88G>A | NP_001265067.1:p.Val30Met | |
| XR_001746952.2:n.82+292C>T | ||
| NM_001114753.3:c.634G>A MANE Select | NP_001108225.1:p.Val212Met | |
| NM_001278138.2:c.88G>A | NP_001265067.1:p.Val30Met |