Linked Data
MyVariant Identifiers:
chr6:g.3154988G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.3154754G>C , CM000668.2:g.3154754G>C | GRCh38 |
| NC_000006.11:g.3154988G>C , CM000668.1:g.3154988G>C | GRCh37 |
| NC_000006.10:g.3099987G>C | NCBI36 |
| NG_042223.1:g.7796C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000333628.4:c.447C>G MANE Select | ENSP00000369703.2:p.Thr149= | |
| ENST00000679400.1:n.503C>G | ||
| ENST00000679907.1:n.835C>G | ||
| ENST00000680036.1:n.1229C>G | ||
| ENST00000680967.1:n.1537C>G | ||
| ENST00000333628.3:c.447C>G | ENSP00000369703.2:p.Thr149= | |
| ENST00000489942.1:n.642C>G | ||
| NM_001069.2:c.447C>G | NP_001060.1:p.Thr149= | |
| NM_001310315.1:c.192C>G | NP_001297244.1:p.Thr64= | |
| NM_001069.3:c.447C>G MANE Select | NP_001060.1:p.Thr149= | |
| NM_001310315.2:c.192C>G | NP_001297244.1:p.Thr64= |