Linked Data
MyVariant Identifiers:
chr6:g.3154847T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.3154613T>G , CM000668.2:g.3154613T>G | GRCh38 |
| NC_000006.11:g.3154847T>G , CM000668.1:g.3154847T>G | GRCh37 |
| NC_000006.10:g.3099846T>G | NCBI36 |
| NG_042223.1:g.7937A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000333628.4:c.588A>C MANE Select | ENSP00000369703.2:p.Thr196= | |
| ENST00000679400.1:n.644A>C | ||
| ENST00000679907.1:n.976A>C | ||
| ENST00000680036.1:n.1370A>C | ||
| ENST00000680967.1:n.1678A>C | ||
| ENST00000333628.3:c.588A>C | ENSP00000369703.2:p.Thr196= | |
| ENST00000489942.1:n.783A>C | ||
| NM_001069.2:c.588A>C | NP_001060.1:p.Thr196= | |
| NM_001310315.1:c.333A>C | NP_001297244.1:p.Thr111= | |
| NM_001069.3:c.588A>C MANE Select | NP_001060.1:p.Thr196= | |
| NM_001310315.2:c.333A>C | NP_001297244.1:p.Thr111= |