Linked Data
dbSNP Id:
rs1131015
ExAC:
6:31238010 T / G
gnomAD v2:
6-31238010-T-G
gnomAD v3:
6-31270233-T-G
gnomAD v4:
6-31270233-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31270233T>G , CM000668.2:g.31270233T>G | GRCh38 |
| NC_000006.11:g.31238010T>G , CM000668.1:g.31238010T>G | GRCh37 |
| NC_000006.10:g.31345989T>G | NCBI36 |
| NG_029422.2:g.6899A>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000376228.10:c.872A>C MANE Select | ENSP00000365402.5:p.Gln291Pro | |
| ENST00000376228.9:c.872A>C | ENSP00000365402.5:p.Gln291Pro | |
| ENST00000376237.8:c.*459A>C | ENSP00000365412.4:n.*459A>C | |
| ENST00000383329.7:c.872A>C | ENSP00000372819.3:p.Gln291Pro | |
| ENST00000415537.1:c.763A>C | ||
| ENST00000470363.5:n.190A>C | ||
| ENST00000487245.5:n.1231A>C | ||
| ENST00000495835.1:n.1061A>C | ||
| NM_002117.5:c.872A>C | NP_002108.4:p.Gln291Pro | |
| NM_002117.6:c.872A>C MANE Select | NP_002108.4:p.Gln291Pro |