Linked Data
ClinVar Variation Id:
178608
dbSNP Id:
rs10098224
ExAC:
8:72211364 C / T
gnomAD v2:
8-72211364-C-T
gnomAD v3:
8-71299129-C-T
gnomAD v4:
8-71299129-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.71299129C>T , CM000670.2:g.71299129C>T | GRCh38 |
| NC_000008.10:g.72211364C>T , CM000670.1:g.72211364C>T | GRCh37 |
| NC_000008.9:g.72373918C>T | NCBI36 |
| NG_011735.2:g.68104G>A | |
| NG_011735.3:g.254002G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000340726.8:c.744G>A MANE Select | ENSP00000342626.3:p.Thr248= | |
| ENST00000388741.7:c.642G>A | ENSP00000373393.2:p.Thr214= | |
| ENST00000419131.6:c.729G>A | ENSP00000410176.1:p.Thr243= | |
| ENST00000465115.6:c.*23G>A | ENSP00000428391.1:n.*23G>A | |
| ENST00000496494.6:n.1207G>A | ||
| ENST00000642391.1:c.*511G>A | ENSP00000496700.1:n.*511G>A | |
| ENST00000643681.1:c.831G>A | ENSP00000495390.1:p.Thr277= | |
| ENST00000644229.1:c.816G>A | ENSP00000494568.1:p.Thr272= | |
| ENST00000644712.1:c.813G>A | ENSP00000496188.1:p.Thr271= | |
| ENST00000645793.1:c.744G>A | ENSP00000496255.1:p.Thr248= | |
| ENST00000647540.1:c.744G>A | ENSP00000494438.1:p.Thr248= | |
| ENST00000303824.11:c.726G>A | ENSP00000303221.7:p.Thr242= | |
| ENST00000340726.7:c.744G>A | ENSP00000342626.3:p.Thr248= | |
| ENST00000388740.4:c.645G>A | ENSP00000373392.3:p.Thr215= | |
| ENST00000388741.6:c.642G>A | ENSP00000373393.2:p.Thr214= | |
| ENST00000388742.8:c.744G>A | ENSP00000373394.4:p.Thr248= | |
| ENST00000388743.6:c.741G>A | ENSP00000373395.2:p.Thr247= | |
| ENST00000419131.5:c.729G>A | ENSP00000410176.1:p.Thr243= | |
| ENST00000465115.5:c.*23G>A | ENSP00000428391.1:n.*23G>A | |
| ENST00000496494.5:n.1239G>A | ||
| NM_000503.5:c.744G>A | NP_000494.2:p.Thr248= | |
| NM_001288574.1:c.726G>A | NP_001275503.1:p.Thr242= | |
| NM_001288575.1:c.378G>A | NP_001275504.1:p.Thr126= | |
| NM_172058.3:c.744G>A | NP_742055.1:p.Thr248= | |
| NM_172059.3:c.729G>A | NP_742056.1:p.Thr243= | |
| NM_172060.3:c.645G>A | NP_742057.1:p.Thr215= | |
| XM_011517481.1:c.816G>A | XP_011515783.1:p.Thr272= | |
| XM_011517482.1:c.831G>A | XP_011515784.1:p.Thr277= | |
| XM_011517483.1:c.741G>A | XP_011515785.1:p.Thr247= | |
| XM_011517484.1:c.729G>A | XP_011515786.1:p.Thr243= | |
| XM_011517485.1:c.744G>A | XP_011515787.1:p.Thr248= | |
| XM_011517486.1:c.744G>A | XP_011515788.1:p.Thr248= | |
| XM_011517487.1:c.744G>A | XP_011515789.1:p.Thr248= | |
| XM_011517488.1:c.741G>A | XP_011515790.1:p.Thr247= | |
| XM_011517489.1:c.681G>A | XP_011515791.1:p.Thr227= | |
| XM_011517490.1:c.645G>A | XP_011515792.1:p.Thr215= | |
| XM_011517491.1:c.645G>A | XP_011515793.1:p.Thr215= | |
| XM_011517492.1:c.393G>A | XP_011515794.1:p.Thr131= | |
| NM_172059.4:c.816G>A | NP_742056.2:p.Thr272= | |
| XM_011517483.2:c.741G>A | XP_011515785.1:p.Thr247= | |
| XM_011517484.3:c.816G>A | XP_011515786.2:p.Thr272= | |
| XM_017013201.1:c.831G>A | XP_016868690.1:p.Thr277= | |
| XM_017013202.1:c.831G>A | XP_016868691.1:p.Thr277= | |
| XM_017013203.2:c.828G>A | XP_016868692.1:p.Thr276= | |
| XM_017013204.2:c.813G>A | XP_016868693.1:p.Thr271= | |
| XM_017013205.2:c.831G>A | XP_016868694.1:p.Thr277= | |
| XM_017013206.1:c.744G>A | XP_016868695.1:p.Thr248= | |
| XM_017013207.2:c.831G>A | XP_016868696.1:p.Thr277= | |
| XM_017013208.2:c.741G>A | XP_016868697.1:p.Thr247= | |
| XM_017013210.2:c.813G>A | XP_016868699.1:p.Thr271= | |
| XM_017013211.2:c.681G>A | XP_016868700.1:p.Thr227= | |
| XM_017013212.2:c.645G>A | XP_016868701.1:p.Thr215= | |
| XM_017013213.1:c.393G>A | XP_016868702.1:p.Thr131= | |
| NM_000503.6:c.744G>A MANE Select | NP_000494.2:p.Thr248= | |
| NM_001288574.2:c.726G>A | NP_001275503.1:p.Thr242= | |
| NM_001288575.2:c.378G>A | NP_001275504.1:p.Thr126= | |
| NM_001370333.1:c.831G>A | NP_001357262.1:p.Thr277= | |
| NM_001370334.1:c.744G>A | NP_001357263.1:p.Thr248= | |
| NM_001370335.1:c.744G>A | NP_001357264.1:p.Thr248= | |
| NM_001370336.1:c.813G>A | NP_001357265.1:p.Thr271= | |
| NM_172058.4:c.744G>A | NP_742055.1:p.Thr248= | |
| NM_172059.5:c.816G>A | NP_742056.2:p.Thr272= |