Linked Data
MyVariant Identifiers:
chr6:g.31236949G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31269172G>C , CM000668.2:g.31269172G>C | GRCh38 |
| NC_000006.11:g.31236949G>C , CM000668.1:g.31236949G>C | GRCh37 |
| NC_000006.10:g.31344928G>C | NCBI36 |
| NG_029422.2:g.7960C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000376228.10:c.1098C>G MANE Select | ENSP00000365402.5:p.Ala366= | |
| ENST00000376228.9:c.1098C>G | ENSP00000365402.5:p.Ala366= | |
| ENST00000376237.8:c.*685C>G | ENSP00000365412.4:n.*685C>G | |
| ENST00000383329.7:c.1116C>G | ENSP00000372819.3:p.Ala372= | |
| ENST00000466892.5:n.331C>G | ||
| ENST00000470363.5:n.856C>G | ||
| ENST00000487245.5:n.1457C>G | ||
| NM_002117.5:c.1098C>G | NP_002108.4:p.Ala366= | |
| NM_002117.6:c.1098C>G MANE Select | NP_002108.4:p.Ala366= |