Linked Data
MyVariant Identifiers:
chr6:g.151936586T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.151615451T>A , CM000668.2:g.151615451T>A | GRCh38 |
| NC_000006.11:g.151936586T>A , CM000668.1:g.151936586T>A | GRCh37 |
| NC_000006.10:g.151978279T>A | NCBI36 |
| NG_021198.1:g.126412T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000239374.8:c.1719T>A MANE Select | ENSP00000239374.6:p.Thr573= | |
| ENST00000239374.7:c.1719T>A | ENSP00000239374.6:p.Thr573= | |
| ENST00000537358.1:n.505T>A | ||
| NM_025059.3:c.1719T>A | NP_079335.2:p.Thr573= | |
| XM_011536147.1:c.1737T>A | XP_011534449.1:p.Thr579= | |
| XM_011536148.1:c.1536T>A | XP_011534450.1:p.Thr512= | |
| XM_011536147.2:c.1737T>A | XP_011534449.1:p.Thr579= | |
| XM_011536148.2:c.1536T>A | XP_011534450.1:p.Thr512= | |
| XR_001743865.1:n.129+1270A>T | ||
| NM_025059.4:c.1719T>A MANE Select | NP_079335.2:p.Thr573= |