Linked Data
ClinVar Variation Id:
2887381
ClinVar RCV Id:
RCV003602908
dbSNP Id:
rs753404357
MyVariant Identifiers:
chr17:g.70118956G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.72122815G>A , CM000679.2:g.72122815G>A | GRCh38 |
| NC_000017.10:g.70118956G>A , CM000679.1:g.70118956G>A | GRCh37 |
| NC_000017.9:g.67630551G>A | NCBI36 |
| NG_012490.1:g.6796G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000245479.3:c.528G>A MANE Select | ENSP00000245479.2:p.Pro176= | |
| ENST00000245479.2:c.528G>A | ENSP00000245479.2:p.Pro176= | |
| NM_000346.3:c.528G>A | NP_000337.1:p.Pro176= | |
| NM_000346.4:c.528G>A MANE Select | NP_000337.1:p.Pro176= |