Linked Data
MyVariant Identifiers:
chr6:g.3154985C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.3154751C>T , CM000668.2:g.3154751C>T | GRCh38 |
| NC_000006.11:g.3154985C>T , CM000668.1:g.3154985C>T | GRCh37 |
| NC_000006.10:g.3099984C>T | NCBI36 |
| NG_042223.1:g.7799G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000333628.4:c.450G>A MANE Select | ENSP00000369703.2:p.Leu150= | |
| ENST00000679400.1:n.506G>A | ||
| ENST00000679907.1:n.838G>A | ||
| ENST00000680036.1:n.1232G>A | ||
| ENST00000680967.1:n.1540G>A | ||
| ENST00000333628.3:c.450G>A | ENSP00000369703.2:p.Leu150= | |
| ENST00000489942.1:n.645G>A | ||
| NM_001069.2:c.450G>A | NP_001060.1:p.Leu150= | |
| NM_001310315.1:c.195G>A | NP_001297244.1:p.Leu65= | |
| NM_001069.3:c.450G>A MANE Select | NP_001060.1:p.Leu150= | |
| NM_001310315.2:c.195G>A | NP_001297244.1:p.Leu65= |