Linked Data
MyVariant Identifiers:
chr6:g.3154790C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.3154556C>A , CM000668.2:g.3154556C>A | GRCh38 |
| NC_000006.11:g.3154790C>A , CM000668.1:g.3154790C>A | GRCh37 |
| NC_000006.10:g.3099789C>A | NCBI36 |
| NG_042223.1:g.7994G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000333628.4:c.645G>T MANE Select | ENSP00000369703.2:p.Leu215= | |
| ENST00000679400.1:n.701G>T | ||
| ENST00000679907.1:n.1033G>T | ||
| ENST00000680036.1:n.1427G>T | ||
| ENST00000680967.1:n.1735G>T | ||
| ENST00000333628.3:c.645G>T | ENSP00000369703.2:p.Leu215= | |
| NM_001069.2:c.645G>T | NP_001060.1:p.Leu215= | |
| NM_001310315.1:c.390G>T | NP_001297244.1:p.Leu130= | |
| NM_001069.3:c.645G>T MANE Select | NP_001060.1:p.Leu215= | |
| NM_001310315.2:c.390G>T | NP_001297244.1:p.Leu130= |