gnomAD v2:
gnomAD v4:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.70430388C>T , CM000663.2:g.70430388C>T | GRCh38 |
| NC_000001.10:g.70896071C>T , CM000663.1:g.70896071C>T | GRCh37 |
| NC_000001.9:g.70668659C>T | NCBI36 |
| NG_008041.1:g.24117C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370938.8:c.718C>T MANE Select | ENSP00000359976.3:p.Gln240Ter | |
| ENST00000346806.2:c.586C>T | ENSP00000311554.2:p.Gln196Ter | |
| ENST00000370938.7:c.718C>T | ENSP00000359976.3:p.Gln240Ter | |
| ENST00000411986.6:c.622C>T | ENSP00000413407.2:p.Gln208Ter | |
| ENST00000464926.1:n.766C>T | ||
| NM_001190463.1:c.622C>T | NP_001177392.1:p.Gln208Ter | |
| NM_001902.5:c.718C>T | NP_001893.2:p.Gln240Ter | |
| NM_153742.4:c.586C>T | NP_714964.2:p.Gln196Ter | |
| XM_005270509.2:c.391C>T | XP_005270566.1:p.Gln131Ter | |
| XM_011540787.1:c.148C>T | XP_011539089.1:p.Gln50Ter | |
| XM_005270509.3:c.391C>T | XP_005270566.1:p.Gln131Ter | |
| XM_017000416.2:c.148C>T | XP_016855905.1:p.Gln50Ter | |
| NM_001902.6:c.718C>T MANE Select | NP_001893.2:p.Gln240Ter | |
| NM_001190463.2:c.622C>T | NP_001177392.1:p.Gln208Ter | |
| NM_153742.5:c.586C>T | NP_714964.2:p.Gln196Ter |