Linked Data
MyVariant Identifiers:
chr6:g.3154889G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.3154655G>T , CM000668.2:g.3154655G>T | GRCh38 |
| NC_000006.11:g.3154889G>T , CM000668.1:g.3154889G>T | GRCh37 |
| NC_000006.10:g.3099888G>T | NCBI36 |
| NG_042223.1:g.7895C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000333628.4:c.546C>A MANE Select | ENSP00000369703.2:p.Pro182= | |
| ENST00000679400.1:n.602C>A | ||
| ENST00000679907.1:n.934C>A | ||
| ENST00000680036.1:n.1328C>A | ||
| ENST00000680967.1:n.1636C>A | ||
| ENST00000333628.3:c.546C>A | ENSP00000369703.2:p.Pro182= | |
| ENST00000489942.1:n.741C>A | ||
| NM_001069.2:c.546C>A | NP_001060.1:p.Pro182= | |
| NM_001310315.1:c.291C>A | NP_001297244.1:p.Pro97= | |
| NM_001069.3:c.546C>A MANE Select | NP_001060.1:p.Pro182= | |
| NM_001310315.2:c.291C>A | NP_001297244.1:p.Pro97= |