Linked Data
ClinVar Variation Id:
25069
ClinVar RCV Id:
RCV000021994
dbSNP Id:
rs397514408
gnomAD v4:
3-15645108-T-C
PubMed:
PMID:26810761
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.15645108T>C , CM000665.2:g.15645108T>C | GRCh38 |
| NC_000003.11:g.15686615T>C , CM000665.1:g.15686615T>C | GRCh37 |
| NC_000003.10:g.15661619T>C | NCBI36 |
| NG_008019.1:g.48361T>C | |
| NG_008019.2:g.48757T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000436193.6:c.1192T>C | ENSP00000394277.2:p.Cys398Arg | |
| ENST00000671928.2:c.399+3051T>C | ENSP00000500069.2:n.399+3051T>C | |
| ENST00000672892.2:c.1015+177T>C | ENSP00000499944.2:n.1015+177T>C | |
| ENST00000303498.10:c.1192T>C | ENSP00000306477.6:p.Cys398Arg | |
| ENST00000427382.2:c.1192T>C | ENSP00000397113.2:p.Cys398Arg | |
| ENST00000437172.6:c.1192T>C | ENSP00000400995.2:p.Cys398Arg | |
| ENST00000449107.7:c.1192T>C | ENSP00000388212.2:p.Cys398Arg | |
| ENST00000643237.3:c.1192T>C MANE Select | ENSP00000495254.2:p.Cys398Arg | |
| ENST00000646371.1:c.1192T>C | ENSP00000495866.1:p.Cys398Arg | |
| ENST00000671928.1:c.165+3051T>C | ENSP00000500069.1:n.165+3051T>C | |
| ENST00000672065.1:c.1252T>C | ENSP00000500403.1:p.Cys418Arg | |
| ENST00000672112.1:c.1258T>C | ENSP00000500193.1:p.Cys420Arg | |
| ENST00000672141.1:c.399+3051T>C | ENSP00000500210.1:n.399+3051T>C | |
| ENST00000672427.1:c.1015+177T>C | ENSP00000500131.1:n.1015+177T>C | |
| ENST00000672760.1:c.399+3051T>C | ENSP00000500530.1:n.399+3051T>C | |
| ENST00000672892.1:c.793+177T>C | ENSP00000499944.1:n.793+177T>C | |
| ENST00000673467.1:c.399+3051T>C | ENSP00000500288.1:n.399+3051T>C | |
| ENST00000673620.1:c.399+3051T>C | ENSP00000500325.1:n.399+3051T>C | |
| ENST00000303498.9:c.1252T>C | ENSP00000306477.5:p.Cys418Arg | |
| ENST00000383778.5:c.1192T>C | ENSP00000373288.4:p.Cys398Arg | |
| ENST00000437172.5:c.1258T>C | ENSP00000400995.1:p.Cys420Arg | |
| ENST00000449107.5:c.1258T>C | ENSP00000388212.1:p.Cys420Arg | |
| NM_000060.3:c.1252T>C | NP_000051.1:p.Cys418Arg | |
| NM_001281723.1:c.1258T>C | NP_001268652.1:p.Cys420Arg | |
| NM_001281724.1:c.1258T>C | NP_001268653.1:p.Cys420Arg | |
| NM_001281725.1:c.1192T>C | NP_001268654.1:p.Cys398Arg | |
| XM_006713314.2:c.1192T>C | XP_006713377.1:p.Cys398Arg | |
| XM_011534041.1:c.1192T>C | XP_011532343.1:p.Cys398Arg | |
| NM_000060.4:c.1252T>C | NP_000051.1:p.Cys418Arg | |
| NM_001281723.2:c.1258T>C | NP_001268652.1:p.Cys420Arg | |
| NM_001281724.2:c.1258T>C | NP_001268653.1:p.Cys420Arg | |
| NM_001281725.2:c.1192T>C | NP_001268654.1:p.Cys398Arg | |
| NM_001323582.1:c.1192T>C | NP_001310511.1:p.Cys398Arg | |
| XM_011534041.2:c.1192T>C | XP_011532343.1:p.Cys398Arg | |
| XM_017007088.1:c.1192T>C | XP_016862577.1:p.Cys398Arg | |
| XM_024453724.1:c.1192T>C | XP_024309492.1:p.Cys398Arg | |
| NM_001281723.3:c.1192T>C | NP_001268652.2:p.Cys398Arg | |
| NM_001281724.3:c.1192T>C | NP_001268653.2:p.Cys398Arg | |
| NM_001370658.1:c.1192T>C MANE Select | NP_001357587.1:p.Cys398Arg | |
| NM_001370752.1:c.1015+177T>C | NP_001357681.1:n.1015+177T>C | |
| NM_001370753.1:c.399+3051T>C | NP_001357682.1:n.399+3051T>C | |
| NM_001281726.2:c.*2970T>C | NP_001268655.2:n.*2970T>C |