Linked Data
ClinVar Variation Id:
2052977
ClinVar RCV Id:
RCV002918956
gnomAD v4:
10-68231645-C-T
MyVariant Identifiers:
chr10:g.69991402C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.68231645C>T , CM000672.2:g.68231645C>T | GRCh38 |
| NC_000010.10:g.69991402C>T , CM000672.1:g.69991402C>T | GRCh37 |
| NC_000010.9:g.69661408C>T | NCBI36 |
| NG_031934.1:g.5469G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373673.5:c.33G>A MANE Select | ENSP00000362777.3:p.Ala11= | |
| ENST00000373673.4:c.33G>A | ENSP00000362777.3:p.Ala11= | |
| NM_145178.3:c.33G>A | NP_660161.1:p.Ala11= | |
| NM_145178.4:c.33G>A MANE Select | NP_660161.1:p.Ala11= |