Linked Data
ClinVar Variation Id:
1046712
ClinVar RCV Id:
RCV001351305
dbSNP Id:
rs1851091277
gnomAD v4:
11-36593762-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.36593762G>A , CM000673.2:g.36593762G>A | GRCh38 |
| NC_000011.9:g.36615312G>A , CM000673.1:g.36615312G>A | GRCh37 |
| NC_000011.8:g.36571888G>A | NCBI36 |
| NG_007573.1:g.9475C>T , LRG_99:g.9475C>T | |
| NG_033154.1:g.4270G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000527033.6:c.407C>T | ENSP00000436895.2:p.Ala136Val | |
| ENST00000529083.2:c.407C>T | ENSP00000436327.2:p.Ala136Val | |
| ENST00000532616.2:c.407C>T | ENSP00000432174.2:p.Ala136Val | |
| ENST00000311485.8:c.407C>T MANE Select | ENSP00000308620.4:p.Ala136Val | |
| ENST00000311485.7:c.407C>T | ENSP00000308620.3:p.Ala136Val | |
| ENST00000524423.1:n.131+4340C>T | ||
| ENST00000529083.1:c.407C>T | ENSP00000436327.1:p.Ala136Val | |
| ENST00000618712.4:c.407C>T | ENSP00000478672.1:p.Ala136Val | |
| NM_000536.3:c.407C>T | NP_000527.2:p.Ala136Val | |
| NM_001243785.1:c.407C>T | NP_001230714.1:p.Ala136Val | |
| NM_001243786.1:c.407C>T | NP_001230715.1:p.Ala136Val | |
| NM_000536.4:c.407C>T MANE Select | NP_000527.2:p.Ala136Val | |
| NM_001243785.2:c.407C>T | NP_001230714.1:p.Ala136Val | |
| NM_001243786.2:c.407C>T | NP_001230715.1:p.Ala136Val |