Linked Data
dbSNP Id:
rs1377682176
gnomAD v2:
3-183855708-A-G
gnomAD v3:
3-184137920-A-G
gnomAD v4:
3-184137920-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.184137920A>G , CM000665.2:g.184137920A>G | GRCh38 |
| NC_000003.11:g.183855708A>G , CM000665.1:g.183855708A>G | GRCh37 |
| NC_000003.10:g.185338402A>G | NCBI36 |
| NG_015826.1:g.7899A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000465218.3:n.552A>G | ||
| ENST00000468748.7:n.512A>G | ||
| ENST00000484154.2:n.1150A>G | ||
| ENST00000491008.6:n.1277A>G | ||
| ENST00000492226.2:n.526A>G | ||
| ENST00000492773.6:c.261A>G | ||
| ENST00000647636.1:c.529A>G | ENSP00000497505.1:p.Asn177Asp | |
| ENST00000647909.1:c.553A>G | ENSP00000498164.1:p.Asn185Asp | |
| ENST00000648145.1:c.297A>G | ||
| ENST00000648189.1:c.279A>G | ||
| ENST00000648256.1:c.478A>G | ENSP00000497356.1:p.Asn160Asp | |
| ENST00000648314.1:c.529A>G | ENSP00000496920.1:p.Asn177Asp | |
| ENST00000648599.1:c.529A>G | ENSP00000497159.1:p.Asn177Asp | |
| ENST00000648630.1:c.523A>G | ENSP00000497887.1:p.Asn175Asp | |
| ENST00000648682.1:c.529A>G | ENSP00000498185.1:p.Asn177Asp | |
| ENST00000648882.1:c.*355A>G | ENSP00000497603.1:n.*355A>G | |
| ENST00000648890.1:c.529A>G | ENSP00000497503.1:p.Asn177Asp | |
| ENST00000648915.2:c.529A>G MANE Select | ENSP00000497160.1:p.Asn177Asp | |
| ENST00000649545.1:c.263A>G | ||
| ENST00000649688.1:c.529A>G | ENSP00000497097.1:p.Asn177Asp | |
| ENST00000649814.1:n.578A>G | ||
| ENST00000650244.1:c.674A>G | ENSP00000497227.1:n.674A>G | |
| ENST00000650270.1:c.396A>G | ||
| ENST00000273783.7:c.529A>G | ENSP00000273783.3:p.Asn177Asp | |
| ENST00000432982.5:c.245+1245A>G | ||
| ENST00000444495.1:c.529A>G | ENSP00000409142.1:p.Asn177Asp | |
| ENST00000481054.5:n.530A>G | ||
| ENST00000491008.5:n.493A>G | ||
| ENST00000491144.5:n.969A>G | ||
| ENST00000498831.1:n.484A>G | ||
| NM_003907.2:c.529A>G | NP_003898.2:p.Asn177Asp | |
| XR_924208.1:n.1480A>G | ||
| NM_003907.3:c.529A>G MANE Select | NP_003898.2:p.Asn177Asp | |
| XM_011513266.3:c.-373A>G | XP_011511568.1:n.-373A>G | |
| XR_001740352.2:n.892A>G | ||
| XR_001740353.2:n.892A>G | ||
| XR_924208.2:n.892A>G |