Linked Data
MyVariant Identifiers:
chr6:g.151936688A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.151615553A>G , CM000668.2:g.151615553A>G | GRCh38 |
| NC_000006.11:g.151936688A>G , CM000668.1:g.151936688A>G | GRCh37 |
| NC_000006.10:g.151978381A>G | NCBI36 |
| NG_021198.1:g.126514A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000239374.8:c.1821A>G MANE Select | ENSP00000239374.6:p.Glu607= | |
| ENST00000239374.7:c.1821A>G | ENSP00000239374.6:p.Glu607= | |
| NM_025059.3:c.1821A>G | NP_079335.2:p.Glu607= | |
| XM_011536147.1:c.1839A>G | XP_011534449.1:p.Glu613= | |
| XM_011536148.1:c.1638A>G | XP_011534450.1:p.Glu546= | |
| XM_011536147.2:c.1839A>G | XP_011534449.1:p.Glu613= | |
| XM_011536148.2:c.1638A>G | XP_011534450.1:p.Glu546= | |
| XR_001743865.1:n.129+1168T>C | ||
| NM_025059.4:c.1821A>G MANE Select | NP_079335.2:p.Glu607= |