Linked Data
MyVariant Identifiers:
chr6:g.151936730G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.151615595G>A , CM000668.2:g.151615595G>A | GRCh38 |
| NC_000006.11:g.151936730G>A , CM000668.1:g.151936730G>A | GRCh37 |
| NC_000006.10:g.151978423G>A | NCBI36 |
| NG_021198.1:g.126556G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000239374.8:c.1863G>A MANE Select | ENSP00000239374.6:p.Arg621= | |
| ENST00000239374.7:c.1863G>A | ENSP00000239374.6:p.Arg621= | |
| NM_025059.3:c.1863G>A | NP_079335.2:p.Arg621= | |
| XM_011536147.1:c.1881G>A | XP_011534449.1:p.Arg627= | |
| XM_011536148.1:c.1680G>A | XP_011534450.1:p.Arg560= | |
| XM_011536147.2:c.1881G>A | XP_011534449.1:p.Arg627= | |
| XM_011536148.2:c.1680G>A | XP_011534450.1:p.Arg560= | |
| XR_001743865.1:n.129+1126C>T | ||
| NM_025059.4:c.1863G>A MANE Select | NP_079335.2:p.Arg621= |