Linked Data
ClinVar Variation Id:
2914736
dbSNP Id:
rs75307879
gnomAD v3:
15-73323114-C-A
gnomAD v4:
15-73323114-C-A
MyVariant Identifiers:
chr15:g.73615455C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.73323114C>A , CM000677.2:g.73323114C>A | GRCh38 |
| NC_000015.9:g.73615455C>A , CM000677.1:g.73615455C>A | GRCh37 |
| NC_000015.8:g.71402508C>A | NCBI36 |
| NG_009063.1:g.51151G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261917.4:c.2979G>T MANE Select | ENSP00000261917.3:p.Thr993= | |
| ENST00000261917.3:c.2979G>T | ENSP00000261917.3:p.Thr993= | |
| NM_005477.2:c.2979G>T | NP_005468.1:p.Thr993= | |
| XM_011521148.1:c.1761G>T | XP_011519450.1:p.Thr587= | |
| XM_011521148.2:c.1761G>T | XP_011519450.1:p.Thr587= | |
| NM_005477.3:c.2979G>T MANE Select | NP_005468.1:p.Thr993= |