Linked Data
ClinVar Variation Id:
381664
dbSNP Id:
rs144993986
ExAC:
9:34649484 C / T
gnomAD v2:
9-34649484-C-T
gnomAD v3:
9-34649487-C-T
gnomAD v4:
9-34649487-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.34649487C>T , CM000671.2:g.34649487C>T | GRCh38 |
| NC_000009.11:g.34649484C>T , CM000671.1:g.34649484C>T | GRCh37 |
| NC_000009.10:g.34639484C>T | NCBI36 |
| NG_009029.1:g.7850C>T | |
| NG_028966.1:g.2303C>T | |
| NG_009029.2:g.7899C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000691183.1:c.*570C>T | ENSP00000509954.1:n.*570C>T | |
| ENST00000378842.8:c.982C>T MANE Select | ENSP00000368119.4:p.Arg328Cys | |
| ENST00000378842.7:c.982C>T | ENSP00000368119.3:p.Arg328Cys | |
| ENST00000450095.6:c.655C>T | ENSP00000401956.2:p.Arg219Cys | |
| ENST00000488412.2:n.566C>T | ||
| ENST00000489643.6:n.1390C>T | ||
| ENST00000554550.5:c.*602C>T | ENSP00000451435.1:n.*602C>T | |
| ENST00000554638.5:n.1454C>T | ||
| ENST00000555020.5:n.1771C>T | ||
| ENST00000555754.1:n.430C>T | ||
| ENST00000556278.1:c.432+1031C>T | ENSP00000451792.1:n.432+1031C>T | |
| ENST00000557706.5:n.1557C>T | ||
| NM_000155.3:c.982C>T | NP_000146.2:p.Arg328Cys | |
| NM_001258332.1:c.655C>T | NP_001245261.1:p.Arg219Cys | |
| NM_000155.4:c.982C>T MANE Select | NP_000146.2:p.Arg328Cys | |
| NM_001258332.2:c.655C>T | NP_001245261.1:p.Arg219Cys |