Linked Data
ClinVar Variation Id:
2063753
ClinVar RCV Id:
RCV002923922
MyVariant Identifiers:
chr14:g.24728913G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.24259707G>T , CM000676.2:g.24259707G>T | GRCh38 |
| NC_000014.8:g.24728913G>T , CM000676.1:g.24728913G>T | GRCh37 |
| NC_000014.7:g.23798753G>T | NCBI36 |
| NG_007150.1:g.8460C>A | |
| NG_007150.2:g.8460C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000206765.11:c.981C>A MANE Select | ENSP00000206765.6:p.Ala327= | |
| ENST00000206765.10:c.981C>A | ENSP00000206765.6:p.Ala327= | |
| ENST00000544573.5:c.-28-1319C>A | ENSP00000439446.1:n.-28-1319C>A | |
| ENST00000559136.1:c.54C>A | ENSP00000453337.1:p.Ala18= | |
| NM_000359.2:c.981C>A | NP_000350.1:p.Ala327= | |
| NM_000359.3:c.981C>A MANE Select | NP_000350.1:p.Ala327= |