Linked Data
ClinVar Variation Id:
17024
dbSNP Id:
rs28931592
ExAC:
13:20763245 T / A
gnomAD v2:
13-20763245-T-A
gnomAD v3:
13-20189106-T-A
gnomAD v4:
13-20189106-T-A
PubMed:
PMID:12239718
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.20189106T>A , CM000675.2:g.20189106T>A | GRCh38 |
| NC_000013.10:g.20763245T>A , CM000675.1:g.20763245T>A | GRCh37 |
| NC_000013.9:g.19661245T>A | NCBI36 |
| NG_008358.1:g.8870A>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000382844.2:c.476A>T | ENSP00000372295.1:p.Asp159Val | |
| ENST00000382848.5:c.476A>T MANE Select | ENSP00000372299.4:p.Asp159Val | |
| ENST00000382844.1:c.476A>T | ENSP00000372295.1:p.Asp159Val | |
| ENST00000382848.4:c.476A>T | ENSP00000372299.4:p.Asp159Val | |
| NM_004004.5:c.476A>T | NP_003995.2:p.Asp159Val | |
| XM_011535049.1:c.476A>T | XP_011533351.1:p.Asp159Val | |
| XM_011535049.2:c.476A>T | XP_011533351.1:p.Asp159Val | |
| NM_004004.6:c.476A>T MANE Select | NP_003995.2:p.Asp159Val |