Linked Data
ClinVar Variation Id:
363639
dbSNP Id:
rs79700717
gnomAD v2:
8-72110870-C-A
gnomAD v3:
8-71198635-C-A
gnomAD v4:
8-71198635-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.71198635C>A , CM000670.2:g.71198635C>A | GRCh38 |
| NC_000008.10:g.72110870C>A , CM000670.1:g.72110870C>A | GRCh37 |
| NC_000008.9:g.72273424C>A | NCBI36 |
| NG_011735.2:g.168598G>T | |
| NG_011735.3:g.354496G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000340726.8:c.*705G>T MANE Select | ENSP00000342626.3:n.*705G>T | |
| ENST00000419131.6:c.*705G>T | ENSP00000410176.1:n.*705G>T | |
| ENST00000465115.6:c.*1763G>T | ENSP00000428391.1:n.*1763G>T | |
| ENST00000642391.1:c.*2161G>T | ENSP00000496700.1:n.*2161G>T | |
| ENST00000643681.1:c.*705G>T | ENSP00000495390.1:n.*705G>T | |
| ENST00000644229.1:c.*705G>T | ENSP00000494568.1:n.*705G>T | |
| ENST00000644424.1:n.1554G>T | ||
| ENST00000644712.1:c.*705G>T | ENSP00000496188.1:n.*705G>T | |
| ENST00000645793.1:c.*705G>T | ENSP00000496255.1:n.*705G>T | |
| ENST00000647540.1:c.*705G>T | ENSP00000494438.1:n.*705G>T | |
| ENST00000303824.11:c.*705G>T | ENSP00000303221.7:n.*705G>T | |
| ENST00000340726.7:c.*705G>T | ENSP00000342626.3:n.*705G>T | |
| ENST00000388740.4:c.*705G>T | ENSP00000373392.3:n.*705G>T | |
| ENST00000388741.6:c.*705G>T | ENSP00000373393.2:n.*705G>T | |
| ENST00000388742.8:c.*705G>T | ENSP00000373394.4:n.*705G>T | |
| ENST00000465115.5:c.*1763G>T | ENSP00000428391.1:n.*1763G>T | |
| NM_000503.5:c.*705G>T | NP_000494.2:n.*705G>T | |
| NM_001288574.1:c.*705G>T | NP_001275503.1:n.*705G>T | |
| NM_001288575.1:c.*705G>T | NP_001275504.1:n.*705G>T | |
| NM_172058.3:c.*705G>T | NP_742055.1:n.*705G>T | |
| NM_172059.3:c.*705G>T | NP_742056.1:n.*705G>T | |
| NM_172060.3:c.*705G>T | NP_742057.1:n.*705G>T | |
| XM_011517481.1:c.*592G>T | XP_011515783.1:n.*592G>T | |
| XM_011517482.1:c.*592G>T | XP_011515784.1:n.*592G>T | |
| XM_011517483.1:c.*705G>T | XP_011515785.1:n.*705G>T | |
| XM_011517484.1:c.*705G>T | XP_011515786.1:n.*705G>T | |
| XM_011517485.1:c.*592G>T | XP_011515787.1:n.*592G>T | |
| XM_011517486.1:c.*592G>T | XP_011515788.1:n.*592G>T | |
| XM_011517487.1:c.*592G>T | XP_011515789.1:n.*592G>T | |
| XM_011517488.1:c.*592G>T | XP_011515790.1:n.*592G>T | |
| XM_011517489.1:c.*592G>T | XP_011515791.1:n.*592G>T | |
| XM_011517490.1:c.*592G>T | XP_011515792.1:n.*592G>T | |
| XM_011517491.1:c.*592G>T | XP_011515793.1:n.*592G>T | |
| XM_011517492.1:c.*592G>T | XP_011515794.1:n.*592G>T | |
| XR_929038.1:n.180-505C>A | ||
| NM_172059.4:c.*705G>T | NP_742056.2:n.*705G>T | |
| XM_011517483.2:c.*705G>T | XP_011515785.1:n.*705G>T | |
| XM_011517484.3:c.*705G>T | XP_011515786.2:n.*705G>T | |
| XM_017013201.1:c.*705G>T | XP_016868690.1:n.*705G>T | |
| XM_017013202.1:c.*705G>T | XP_016868691.1:n.*705G>T | |
| XM_017013203.2:c.*705G>T | XP_016868692.1:n.*705G>T | |
| XM_017013204.2:c.*705G>T | XP_016868693.1:n.*705G>T | |
| XM_017013206.1:c.*705G>T | XP_016868695.1:n.*705G>T | |
| XM_017013207.2:c.*705G>T | XP_016868696.1:n.*705G>T | |
| XM_017013208.2:c.*705G>T | XP_016868697.1:n.*705G>T | |
| XM_017013210.2:c.*705G>T | XP_016868699.1:n.*705G>T | |
| XM_017013211.2:c.*705G>T | XP_016868700.1:n.*705G>T | |
| XM_017013212.2:c.*705G>T | XP_016868701.1:n.*705G>T | |
| XM_017013213.1:c.*705G>T | XP_016868702.1:n.*705G>T | |
| XR_001745954.1:n.4803-505C>A | ||
| NM_000503.6:c.*705G>T MANE Select | NP_000494.2:n.*705G>T | |
| NM_001288574.2:c.*705G>T | NP_001275503.1:n.*705G>T | |
| NM_001288575.2:c.*705G>T | NP_001275504.1:n.*705G>T | |
| NM_001370333.1:c.*705G>T | NP_001357262.1:n.*705G>T | |
| NM_001370334.1:c.*705G>T | NP_001357263.1:n.*705G>T | |
| NM_001370335.1:c.*705G>T | NP_001357264.1:n.*705G>T | |
| NM_001370336.1:c.*705G>T | NP_001357265.1:n.*705G>T | |
| NM_172058.4:c.*705G>T | NP_742055.1:n.*705G>T | |
| NM_172059.5:c.*705G>T | NP_742056.2:n.*705G>T |