Linked Data
MyVariant Identifiers:
chr6:g.31237807G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31270030G>A , CM000668.2:g.31270030G>A | GRCh38 |
| NC_000006.11:g.31237807G>A , CM000668.1:g.31237807G>A | GRCh37 |
| NC_000006.10:g.31345786G>A | NCBI36 |
| NG_029422.2:g.7102C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000376228.10:c.951C>T MANE Select | ENSP00000365402.5:p.Val317= | |
| ENST00000376228.9:c.951C>T | ENSP00000365402.5:p.Val317= | |
| ENST00000376237.8:c.*538C>T | ENSP00000365412.4:n.*538C>T | |
| ENST00000383329.7:c.951C>T | ENSP00000372819.3:p.Val317= | |
| ENST00000470363.5:n.269C>T | ||
| ENST00000487245.5:n.1310C>T | ||
| NM_002117.5:c.951C>T | NP_002108.4:p.Val317= | |
| NM_002117.6:c.951C>T MANE Select | NP_002108.4:p.Val317= |