Linked Data
ClinVar Variation Id:
2930248
ClinVar RCV Id:
RCV003787606
MyVariant Identifiers:
chr5:g.149357629C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.149978066C>A , CM000667.2:g.149978066C>A | GRCh38 |
| NC_000005.9:g.149357629C>A , CM000667.1:g.149357629C>A | GRCh37 |
| NC_000005.8:g.149337822C>A | NCBI36 |
| NG_007147.2:g.19184C>A , LRG_684:g.19184C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000690410.1:n.646C>A | ||
| ENST00000286298.5:c.414C>A MANE Select | ENSP00000286298.4:p.Val138= | |
| ENST00000286298.4:c.414C>A | ENSP00000286298.4:p.Val138= | |
| ENST00000503336.1:c.87C>A | ENSP00000426053.1:p.Val29= | |
| NM_000112.3:c.414C>A , LRG_684t1:c.414C>A | NP_000103.2:p.Val138= | |
| XM_017009191.2:c.414C>A | XP_016864680.1:p.Val138= | |
| NM_000112.4:c.414C>A MANE Select | NP_000103.2:p.Val138= |