Linked Data
ClinVar Variation Id:
533927
dbSNP Id:
rs369693274
ExAC:
16:81399025 G / A
gnomAD v2:
16-81399025-G-A
gnomAD v3:
16-81365420-G-A
gnomAD v4:
16-81365420-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.81365420G>A , CM000678.2:g.81365420G>A | GRCh38 |
| NC_000016.9:g.81399025G>A , CM000678.1:g.81399025G>A | GRCh37 |
| NC_000016.8:g.79956526G>A | NCBI36 |
| NG_009007.1:g.55455G>A , LRG_242:g.55455G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000648349.2:c.*1152G>A | ENSP00000498114.1:n.*1152G>A | |
| ENST00000648994.2:c.1444G>A MANE Select | ENSP00000497351.1:p.Ala482Thr | |
| ENST00000650388.1:c.978G>A | ENSP00000498081.1:n.978G>A | |
| ENST00000567335.1:n.2G>A | ||
| ENST00000568107.2:c.1444G>A | ENSP00000476795.1:p.Ala482Thr | |
| NM_022041.3:c.1444G>A , LRG_242t1:c.1444G>A | NP_071324.1:p.Ala482Thr | |
| XM_017023734.1:c.805G>A | XP_016879223.1:p.Ala269Thr | |
| NM_001377486.1:c.805G>A | NP_001364415.1:p.Ala269Thr | |
| NM_022041.4:c.1444G>A MANE Select | NP_071324.1:p.Ala482Thr |