Linked Data
dbSNP Id:
rs1478315356
gnomAD v2:
3-183855599-G-A
gnomAD v3:
3-184137811-G-A
gnomAD v4:
3-184137811-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.184137811G>A , CM000665.2:g.184137811G>A | GRCh38 |
| NC_000003.11:g.183855599G>A , CM000665.1:g.183855599G>A | GRCh37 |
| NC_000003.10:g.185338293G>A | NCBI36 |
| NG_015826.1:g.7790G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000465218.3:n.529+6G>A | ||
| ENST00000468748.7:n.489+6G>A | ||
| ENST00000484154.2:n.1127+6G>A | ||
| ENST00000491008.6:n.1254+6G>A | ||
| ENST00000492226.2:n.503+6G>A | ||
| ENST00000492773.6:c.238+6G>A | ||
| ENST00000647636.1:c.506+6G>A | ENSP00000497505.1:n.506+6G>A | |
| ENST00000647909.1:c.506+6G>A | ENSP00000498164.1:n.506+6G>A | |
| ENST00000648145.1:c.274+6G>A | ||
| ENST00000648189.1:c.256+6G>A | ||
| ENST00000648256.1:c.455+6G>A | ENSP00000497356.1:n.455+6G>A | |
| ENST00000648314.1:c.506+6G>A | ENSP00000496920.1:n.506+6G>A | |
| ENST00000648599.1:c.506+6G>A | ENSP00000497159.1:n.506+6G>A | |
| ENST00000648630.1:c.500+6G>A | ENSP00000497887.1:n.500+6G>A | |
| ENST00000648682.1:c.506+6G>A | ENSP00000498185.1:n.506+6G>A | |
| ENST00000648882.1:c.*332+6G>A | ENSP00000497603.1:n.*332+6G>A | |
| ENST00000648890.1:c.506+6G>A | ENSP00000497503.1:n.506+6G>A | |
| ENST00000648915.2:c.506+6G>A MANE Select | ENSP00000497160.1:n.506+6G>A | |
| ENST00000649545.1:c.240+6G>A | ||
| ENST00000649688.1:c.506+6G>A | ENSP00000497097.1:n.506+6G>A | |
| ENST00000649814.1:n.555+6G>A | ||
| ENST00000650244.1:c.651+6G>A | ENSP00000497227.1:n.651+6G>A | |
| ENST00000650270.1:c.373+6G>A | ||
| ENST00000273783.7:c.506+6G>A | ENSP00000273783.3:n.506+6G>A | |
| ENST00000432982.5:c.245+1136G>A | ||
| ENST00000444495.1:c.506+6G>A | ENSP00000409142.1:n.506+6G>A | |
| ENST00000481054.5:n.507+6G>A | ||
| ENST00000491008.5:n.470+6G>A | ||
| ENST00000491144.5:n.860G>A | ||
| ENST00000498831.1:n.461+6G>A | ||
| NM_003907.2:c.506+6G>A | NP_003898.2:n.506+6G>A | |
| XR_924208.1:n.1457+6G>A | ||
| NM_003907.3:c.506+6G>A MANE Select | NP_003898.2:n.506+6G>A | |
| XM_011513266.3:c.-396+6G>A | XP_011511568.1:n.-396+6G>A | |
| XR_001740352.2:n.869+6G>A | ||
| XR_001740353.2:n.869+6G>A | ||
| XR_924208.2:n.869+6G>A |