Linked Data
dbSNP Id:
rs375787769
ExAC:
16:1412882 C / A
gnomAD v2:
16-1412882-C-A
gnomAD v3:
16-1362881-C-A
gnomAD v4:
16-1362881-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.1362881C>A , CM000678.2:g.1362881C>A | GRCh38 |
| NC_000016.9:g.1412882C>A , CM000678.1:g.1412882C>A | GRCh37 |
| NC_000016.8:g.1352883C>A | NCBI36 |
| NG_016985.1:g.15983C>A | |
| NG_033129.1:g.56824G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000527168.6:n.897C>A | ||
| ENST00000529110.2:c.882C>A | ENSP00000435349.2:p.His294Gln | |
| ENST00000529957.6:n.856C>A | ||
| ENST00000683366.1:c.*530C>A | ENSP00000507283.1:n.*530C>A | |
| ENST00000683887.1:c.846C>A | ENSP00000506886.1:p.His282Gln | |
| ENST00000684100.1:n.792C>A | ||
| ENST00000684126.1:n.932C>A | ||
| ENST00000684688.1:n.1423C>A | ||
| ENST00000204679.9:c.798C>A MANE Select | ENSP00000204679.4:p.His266Gln | |
| ENST00000204679.8:c.798C>A | ENSP00000204679.4:p.His266Gln | |
| ENST00000527076.1:n.2021C>A | ||
| ENST00000527168.5:n.965C>A | ||
| ENST00000529957.5:n.897C>A | ||
| NM_032520.4:c.798C>A | NP_115909.1:p.His266Gln | |
| XM_017023782.1:c.846C>A | XP_016879271.1:p.His282Gln | |
| XM_017023783.1:c.438C>A | XP_016879272.1:p.His146Gln | |
| NM_032520.5:c.798C>A MANE Select | NP_115909.1:p.His266Gln |