Linked Data
ClinVar Variation Id:
3224203
ClinVar RCV Id:
RCV004518929
MyVariant Identifiers:
chr5:g.172659875C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.173232872C>T , CM000667.2:g.173232872C>T | GRCh38 |
| NC_000005.9:g.172659875C>T , CM000667.1:g.172659875C>T | GRCh37 |
| NC_000005.8:g.172592481C>T | NCBI36 |
| NG_013340.1:g.7441G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000329198.5:c.672G>A MANE Select | ENSP00000327758.4:p.Val224= | |
| ENST00000329198.4:c.672G>A | ENSP00000327758.4:p.Val224= | |
| NM_001166175.1:c.*625G>A | NP_001159647.1:n.*625G>A | |
| NM_001166176.1:c.*471G>A | NP_001159648.1:n.*471G>A | |
| NM_004387.3:c.672G>A | NP_004378.1:p.Val224= | |
| NM_004387.4:c.672G>A MANE Select | NP_004378.1:p.Val224= | |
| NM_001166175.2:c.*625G>A | NP_001159647.1:n.*625G>A | |
| NM_001166176.2:c.*471G>A | NP_001159648.1:n.*471G>A |