Linked Data
ClinVar Variation Id:
1483289
ClinVar RCV Id:
RCV001998706
dbSNP Id:
rs2094220656
gnomAD v3:
19-17834684-G-A
gnomAD v4:
19-17834684-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.17834684G>A , CM000681.2:g.17834684G>A | GRCh38 |
| NC_000019.9:g.17945493G>A , CM000681.1:g.17945493G>A | GRCh37 |
| NC_000019.8:g.17806493G>A | NCBI36 |
| NG_007273.1:g.18308C>T , LRG_77:g.18308C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000526008.6:c.*794C>T | ENSP00000513006.1:n.*794C>T | |
| ENST00000696967.1:n.1414C>T | ||
| ENST00000696970.1:n.892C>T | ||
| ENST00000458235.7:c.2237C>T MANE Select | ENSP00000391676.1:p.Ala746Val | |
| ENST00000458235.5:c.2237C>T | ENSP00000391676.1:p.Ala746Val | |
| ENST00000527031.5:n.2278+2043C>T | ||
| ENST00000527670.5:c.2237C>T | ENSP00000432511.1:p.Ala746Val | |
| ENST00000534444.1:c.2237C>T | ENSP00000436421.1:p.Ala746Val | |
| NM_000215.3:c.2237C>T , LRG_77t1:c.2237C>T | NP_000206.2:p.Ala746Val | |
| XM_005259896.2:c.2366C>T | XP_005259953.1:p.Ala789Val | |
| XM_006722745.2:c.2237C>T | XP_006722808.1:p.Ala746Val | |
| XM_011527990.1:c.2366C>T | XP_011526292.1:p.Ala789Val | |
| XR_430137.2:n.2376C>T | ||
| XM_005259896.3:c.2366C>T | XP_005259953.1:p.Ala789Val | |
| NM_000215.4:c.2237C>T MANE Select | NP_000206.2:p.Ala746Val |