Linked Data
MyVariant Identifiers:
chr6:g.3155030C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.3154796C>T , CM000668.2:g.3154796C>T | GRCh38 |
| NC_000006.11:g.3155030C>T , CM000668.1:g.3155030C>T | GRCh37 |
| NC_000006.10:g.3100029C>T | NCBI36 |
| NG_042223.1:g.7754G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000333628.4:c.405G>A MANE Select | ENSP00000369703.2:p.Leu135= | |
| ENST00000679400.1:n.461G>A | ||
| ENST00000679907.1:n.793G>A | ||
| ENST00000680036.1:n.1187G>A | ||
| ENST00000680967.1:n.1495G>A | ||
| ENST00000333628.3:c.405G>A | ENSP00000369703.2:p.Leu135= | |
| ENST00000489942.1:n.600G>A | ||
| NM_001069.2:c.405G>A | NP_001060.1:p.Leu135= | |
| NM_001310315.1:c.150G>A | NP_001297244.1:p.Leu50= | |
| NM_001069.3:c.405G>A MANE Select | NP_001060.1:p.Leu135= | |
| NM_001310315.2:c.150G>A | NP_001297244.1:p.Leu50= |