Linked Data
ClinVar Variation Id:
2421432
dbSNP Id:
rs368743903
ExAC:
8:41791255 G / A
gnomAD v2:
8-41791255-G-A
gnomAD v3:
8-41933737-G-A
gnomAD v4:
8-41933737-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.41933737G>A , CM000670.2:g.41933737G>A | GRCh38 |
| NC_000008.10:g.41791255G>A , CM000670.1:g.41791255G>A | GRCh37 |
| NC_000008.9:g.41910412G>A | NCBI36 |
| NG_042093.1:g.123290C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265713.8:c.4483C>T MANE Select | ENSP00000265713.2:p.Arg1495Cys | |
| ENST00000396930.4:c.4483C>T | ENSP00000380136.3:p.Arg1495Cys | |
| ENST00000406337.6:c.4489C>T | ENSP00000385888.2:p.Arg1497Cys | |
| ENST00000648335.1:c.4483C>T | ENSP00000497086.1:p.Arg1495Cys | |
| ENST00000649817.1:c.3164C>T | ||
| ENST00000265713.6:c.4483C>T | ENSP00000265713.2:p.Arg1495Cys | |
| ENST00000396930.3:c.4483C>T | ENSP00000380136.3:p.Arg1495Cys | |
| ENST00000406337.5:c.4483C>T | ENSP00000385888.1:p.Arg1495Cys | |
| NM_001099412.1:c.4483C>T | NP_001092882.1:p.Arg1495Cys | |
| NM_001099413.1:c.4483C>T | NP_001092883.1:p.Arg1495Cys | |
| NM_006766.3:c.4483C>T | NP_006757.2:p.Arg1495Cys | |
| NM_006766.4:c.4483C>T | NP_006757.2:p.Arg1495Cys | |
| XM_011544656.1:c.4615C>T | XP_011542958.1:p.Arg1539Cys | |
| XM_011544657.1:c.4615C>T | XP_011542959.1:p.Arg1539Cys | |
| XM_011544658.1:c.4615C>T | XP_011542960.1:p.Arg1539Cys | |
| XM_011544659.1:c.4594C>T | XP_011542961.1:p.Arg1532Cys | |
| XM_011544660.1:c.4501C>T | XP_011542962.1:p.Arg1501Cys | |
| XM_011544656.2:c.4615C>T | XP_011542958.1:p.Arg1539Cys | |
| XM_011544657.3:c.4615C>T | XP_011542959.1:p.Arg1539Cys | |
| XM_011544658.3:c.4615C>T | XP_011542960.1:p.Arg1539Cys | |
| XM_011544659.2:c.4594C>T | XP_011542961.1:p.Arg1532Cys | |
| XM_017013863.1:c.4483C>T | XP_016869352.1:p.Arg1495Cys | |
| XM_017013864.2:c.4483C>T | XP_016869353.1:p.Arg1495Cys | |
| XM_024447285.1:c.3055C>T | XP_024303053.1:p.Arg1019Cys | |
| NM_006766.5:c.4483C>T MANE Select | NP_006757.2:p.Arg1495Cys |