Linked Data
ClinVar Variation Id:
533922
ClinVar RCV Id:
RCV000641249
dbSNP Id:
rs748121633
ExAC:
16:81388130 A / G
gnomAD v2:
16-81388130-A-G
gnomAD v4:
16-81354525-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.81354525A>G , CM000678.2:g.81354525A>G | GRCh38 |
| NC_000016.9:g.81388130A>G , CM000678.1:g.81388130A>G | GRCh37 |
| NC_000016.8:g.79945631A>G | NCBI36 |
| NG_009007.1:g.44560A>G , LRG_242:g.44560A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000648349.2:c.*111A>G | ENSP00000498114.1:n.*111A>G | |
| ENST00000648994.2:c.403A>G MANE Select | ENSP00000497351.1:p.Ile135Val | |
| ENST00000650388.1:c.168-2260A>G | ENSP00000498081.1:n.168-2260A>G | |
| ENST00000674788.1:n.528A>G | ||
| ENST00000568107.2:c.403A>G | ENSP00000476795.1:p.Ile135Val | |
| NM_022041.3:c.403A>G , LRG_242t1:c.403A>G | NP_071324.1:p.Ile135Val | |
| XM_017023734.1:c.-237A>G | XP_016879223.1:n.-237A>G | |
| NM_001377486.1:c.-237A>G | NP_001364415.1:n.-237A>G | |
| NM_022041.4:c.403A>G MANE Select | NP_071324.1:p.Ile135Val |