Linked Data
ClinVar Variation Id:
1047106
dbSNP Id:
rs531489450
ExAC:
15:73660167 C / T
gnomAD v2:
15-73660167-C-T
gnomAD v4:
15-73367826-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.73367826C>T , CM000677.2:g.73367826C>T | GRCh38 |
| NC_000015.9:g.73660167C>T , CM000677.1:g.73660167C>T | GRCh37 |
| NC_000015.8:g.71447220C>T | NCBI36 |
| NG_009063.1:g.6439G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261917.4:c.445G>A MANE Select | ENSP00000261917.3:p.Ala149Thr | |
| ENST00000261917.3:c.445G>A | ENSP00000261917.3:p.Ala149Thr | |
| NM_005477.2:c.445G>A | NP_005468.1:p.Ala149Thr | |
| NM_005477.3:c.445G>A MANE Select | NP_005468.1:p.Ala149Thr |