Linked Data
MyVariant Identifiers:
chr6:g.3155045G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.3154811G>T , CM000668.2:g.3154811G>T | GRCh38 |
| NC_000006.11:g.3155045G>T , CM000668.1:g.3155045G>T | GRCh37 |
| NC_000006.10:g.3100044G>T | NCBI36 |
| NG_042223.1:g.7739C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000333628.4:c.390C>A MANE Select | ENSP00000369703.2:p.Leu130= | |
| ENST00000679400.1:n.446C>A | ||
| ENST00000679907.1:n.778C>A | ||
| ENST00000680036.1:n.1172C>A | ||
| ENST00000680967.1:n.1480C>A | ||
| ENST00000333628.3:c.390C>A | ENSP00000369703.2:p.Leu130= | |
| ENST00000489942.1:n.585C>A | ||
| NM_001069.2:c.390C>A | NP_001060.1:p.Leu130= | |
| NM_001310315.1:c.135C>A | NP_001297244.1:p.Leu45= | |
| NM_001069.3:c.390C>A MANE Select | NP_001060.1:p.Leu130= | |
| NM_001310315.2:c.135C>A | NP_001297244.1:p.Leu45= |