Linked Data
ClinVar Variation Id:
1385152
dbSNP Id:
rs1490522995
gnomAD v2:
15-73660131-G-T
gnomAD v4:
15-73367790-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.73367790G>T , CM000677.2:g.73367790G>T | GRCh38 |
| NC_000015.9:g.73660131G>T , CM000677.1:g.73660131G>T | GRCh37 |
| NC_000015.8:g.71447184G>T | NCBI36 |
| NG_009063.1:g.6475C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261917.4:c.481C>A MANE Select | ENSP00000261917.3:p.Pro161Thr | |
| ENST00000261917.3:c.481C>A | ENSP00000261917.3:p.Pro161Thr | |
| NM_005477.2:c.481C>A | NP_005468.1:p.Pro161Thr | |
| NM_005477.3:c.481C>A MANE Select | NP_005468.1:p.Pro161Thr |