Linked Data
ClinVar Variation Id:
217710
dbSNP Id:
rs863225227
gnomAD v3:
8-93780647-A-G
gnomAD v4:
8-93780647-A-G
PubMed:
PMID:26092869
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.93780647A>G , CM000670.2:g.93780647A>G | GRCh38 |
| NC_000008.10:g.94792875A>G , CM000670.1:g.94792875A>G | GRCh37 |
| NC_000008.9:g.94862051A>G | NCBI36 |
| NG_009190.1:g.30804A>G , LRG_688:g.30804A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000323130.8:c.769A>G | ENSP00000314488.4:p.Met257Val | |
| ENST00000409623.8:c.769A>G | ENSP00000386966.4:p.Met257Val | |
| ENST00000452276.6:c.769A>G | ENSP00000388671.2:p.Met257Val | |
| ENST00000453906.6:c.407-5576A>G | ENSP00000403035.2:n.407-5576A>G | |
| ENST00000520680.2:c.769A>G | ENSP00000428785.2:p.Met257Val | |
| ENST00000521065.2:c.*486A>G | ENSP00000427947.2:n.*486A>G | |
| ENST00000521517.6:c.769A>G | ENSP00000430740.2:p.Met257Val | |
| ENST00000681998.1:c.699A>G | ENSP00000506773.1:n.699A>G | |
| ENST00000682036.1:c.407-5576A>G | ENSP00000508390.1:n.407-5576A>G | |
| ENST00000682577.1:c.699A>G | ENSP00000506963.1:n.699A>G | |
| ENST00000682624.1:c.*343A>G | ENSP00000508343.1:n.*343A>G | |
| ENST00000682700.1:c.769A>G | ENSP00000507627.1:p.Met257Val | |
| ENST00000682744.1:n.307A>G | ||
| ENST00000682804.1:n.592A>G | ||
| ENST00000682837.1:c.524A>G | ENSP00000507920.1:p.His175Arg | |
| ENST00000682935.1:n.2329A>G | ||
| ENST00000682984.1:c.430A>G | ENSP00000507209.1:p.Met144Val | |
| ENST00000683078.1:c.524A>G | ENSP00000506796.1:p.His175Arg | |
| ENST00000683223.1:c.610A>G | ENSP00000507685.1:n.610A>G | |
| ENST00000683238.1:n.2150A>G | ||
| ENST00000683249.1:n.2350A>G | ||
| ENST00000683336.1:c.699A>G | ENSP00000507695.1:n.699A>G | |
| ENST00000683362.1:c.430A>G | ENSP00000506985.1:p.Met144Val | |
| ENST00000683850.1:n.692A>G | ||
| ENST00000683919.1:c.699A>G | ENSP00000507617.1:n.699A>G | |
| ENST00000683953.1:c.680A>G | ENSP00000508375.1:n.680A>G | |
| ENST00000684023.1:c.903A>G | ENSP00000507461.1:n.903A>G | |
| ENST00000684064.1:c.460A>G | ENSP00000508192.1:p.Met154Val | |
| ENST00000684089.1:n.2319A>G | ||
| ENST00000684149.1:c.*105A>G | ENSP00000507943.1:n.*105A>G | |
| ENST00000684416.1:n.728A>G | ||
| ENST00000684540.1:c.699A>G | ENSP00000507987.1:n.699A>G | |
| ENST00000453321.8:c.769A>G MANE Select | ENSP00000389998.3:p.Met257Val | |
| ENST00000323130.7:c.739A>G | ENSP00000314488.3:p.Met247Val | |
| ENST00000409623.7:c.526A>G | ENSP00000386966.3:p.Met176Val | |
| ENST00000425545.2:n.216A>G | ||
| ENST00000452276.5:c.460A>G | ENSP00000388671.1:p.Met154Val | |
| ENST00000453321.7:c.769A>G | ENSP00000389998.3:p.Met257Val | |
| ENST00000453906.5:c.407-5576A>G | ENSP00000403035.1:n.407-5576A>G | |
| ENST00000474944.5:n.427-5576A>G | ||
| ENST00000496213.5:n.234A>G | ||
| NM_001142301.1:c.526A>G , LRG_688t2:c.526A>G | NP_001135773.1:p.Met176Val | |
| NM_153704.5:c.769A>G , LRG_688t1:c.769A>G | NP_714915.3:p.Met257Val | |
| NR_024522.1:n.840A>G | ||
| XM_006716686.2:c.466A>G | XP_006716749.1:p.Met156Val | |
| XM_006716687.2:c.169A>G | XP_006716750.1:p.Met57Val | |
| XM_011517363.1:c.407-5576A>G | XP_011515665.1:n.407-5576A>G | |
| XR_428387.1:n.827A>G | ||
| XR_928360.1:n.827A>G | ||
| XR_928361.1:n.827A>G | ||
| XR_928362.1:n.827A>G | ||
| XM_006716686.4:c.466A>G | XP_006716749.1:p.Met156Val | |
| XM_011517363.3:c.407-5576A>G | XP_011515665.1:n.407-5576A>G | |
| XM_024447326.1:c.115A>G | XP_024303094.1:p.Met39Val | |
| XR_001745619.2:n.810A>G | ||
| XR_428387.2:n.810A>G | ||
| XR_928360.3:n.810A>G | ||
| XR_928362.3:n.810A>G | ||
| NM_153704.6:c.769A>G MANE Select | NP_714915.3:p.Met257Val | |
| NR_024522.2:n.790A>G |