Linked Data
ClinVar Variation Id:
213942
ClinVar RCV Id:
RCV002478687
dbSNP Id:
rs863223856
gnomAD v4:
3-30671943-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.30671943C>T , CM000665.2:g.30671943C>T | GRCh38 |
| NC_000003.11:g.30713435C>T , CM000665.1:g.30713435C>T | GRCh37 |
| NC_000003.10:g.30688439C>T | NCBI36 |
| NG_007490.1:g.70442C>T , LRG_779:g.70442C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000295754.10:c.760C>T MANE Select | ENSP00000295754.5:p.Arg254Cys | |
| ENST00000672866.1:n.2356C>T | ||
| ENST00000295754.9:c.760C>T | ENSP00000295754.5:p.Arg254Cys | |
| ENST00000359013.4:c.835C>T | ENSP00000351905.4:p.Arg279Cys | |
| NM_001024847.2:c.835C>T , LRG_779t1:c.835C>T | NP_001020018.1:p.Arg279Cys | |
| NM_003242.5:c.760C>T | NP_003233.4:p.Arg254Cys | |
| XM_011534043.1:c.787C>T | XP_011532345.1:p.Arg263Cys | |
| XM_011534044.1:c.712C>T | XP_011532346.1:p.Arg238Cys | |
| XM_011534045.1:c.655C>T | XP_011532347.1:p.Arg219Cys | |
| XM_011534043.2:c.787C>T | XP_011532345.1:p.Arg263Cys | |
| XM_011534045.3:c.655C>T | XP_011532347.1:p.Arg219Cys | |
| XM_017007106.1:c.655C>T | XP_016862595.1:p.Arg219Cys | |
| NM_003242.6:c.760C>T MANE Select | NP_003233.4:p.Arg254Cys |