ClinVar Variation:
dbSNP:
gnomAD v2:
gnomAD v4:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.156868201C>T , CM000663.2:g.156868201C>T | GRCh38 |
| NC_000001.10:g.156837993C>T , CM000663.1:g.156837993C>T | GRCh37 |
| NC_000001.9:g.155104617C>T | NCBI36 |
| NG_007493.1:g.57452C>T , LRG_261:g.57452C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000674537.2:c.364C>T | ENSP00000502725.1:p.Gln122Ter | |
| ENST00000392302.7:c.364C>T | ENSP00000376120.3:p.Gln122Ter | |
| ENST00000497019.7:c.364C>T | ENSP00000436804.2:p.Gln122Ter | |
| ENST00000524377.7:c.526C>T MANE Select | ENSP00000431418.1:p.Gln176Ter | |
| ENST00000674537.1:c.364C>T | ENSP00000502725.1:p.Gln122Ter | |
| ENST00000358660.3:c.526C>T | ENSP00000351486.3:p.Gln176Ter | |
| ENST00000368196.7:c.526C>T | ENSP00000357179.3:p.Gln176Ter | |
| ENST00000392302.6:c.436C>T | ENSP00000376120.2:p.Gln146Ter | |
| ENST00000489021.6:n.313-5432C>T | ||
| ENST00000497019.6:c.436C>T | ENSP00000436804.1:p.Gln146Ter | |
| ENST00000524377.5:c.526C>T | ENSP00000431418.1:p.Gln176Ter | |
| ENST00000530298.5:n.584C>T | ||
| NM_001007792.1:c.436C>T , LRG_261t1:c.436C>T | NP_001007793.1:p.Gln146Ter | |
| NM_001012331.1:c.526C>T , LRG_261t2:c.526C>T | NP_001012331.1:p.Gln176Ter | |
| NM_002529.3:c.526C>T , LRG_261t3:c.526C>T | NP_002520.2:p.Gln176Ter | |
| NM_001012331.2:c.526C>T | NP_001012331.1:p.Gln176Ter | |
| NM_002529.4:c.526C>T MANE Select | NP_002520.2:p.Gln176Ter |