Linked Data
ClinVar Variation Id:
745151
dbSNP Id:
rs202207061
ExAC:
15:78894525 G / A
gnomAD v2:
15-78894525-G-A
gnomAD v3:
15-78602183-G-A
gnomAD v4:
15-78602183-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.78602183G>A , CM000677.2:g.78602183G>A | GRCh38 |
| NC_000015.9:g.78894525G>A , CM000677.1:g.78894525G>A | GRCh37 |
| NC_000015.8:g.76681580G>A | NCBI36 |
| NG_016143.1:g.24113C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000326828.6:c.459C>T MANE Select | ENSP00000315602.5:p.Ala153= | |
| ENST00000326828.5:c.459C>T | ENSP00000315602.5:p.Ala153= | |
| ENST00000348639.7:c.459C>T | ENSP00000267951.4:p.Ala153= | |
| ENST00000558903.1:n.166C>T | ||
| ENST00000559658.5:c.459C>T | ENSP00000452896.1:p.Ala153= | |
| NM_000743.4:c.459C>T | NP_000734.2:p.Ala153= | |
| NM_001166694.1:c.459C>T | NP_001160166.1:p.Ala153= | |
| NR_046313.1:n.960C>T | ||
| XM_006720382.1:c.258C>T | XP_006720445.1:p.Ala86= | |
| XM_011521173.1:c.378C>T | XP_011519475.1:p.Ala126= | |
| XM_006720382.3:c.258C>T | XP_006720445.1:p.Ala86= | |
| NM_000743.5:c.459C>T MANE Select | NP_000734.2:p.Ala153= | |
| NM_001166694.2:c.459C>T | NP_001160166.1:p.Ala153= | |
| NR_046313.2:n.661C>T |