Linked Data
MyVariant Identifiers:
chr17:g.42449786G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.44372418G>T , CM000679.2:g.44372418G>T | GRCh38 |
| NC_000017.10:g.42449786G>T , CM000679.1:g.42449786G>T | GRCh37 |
| NC_000017.9:g.39805312G>T | NCBI36 |
| NG_008331.1:g.22088C>A , LRG_479:g.22088C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262407.6:c.3066C>A MANE Select | ENSP00000262407.5:p.Gly1022= | |
| ENST00000648408.1:c.2380C>A | ||
| ENST00000262407.5:c.3066C>A | ENSP00000262407.5:p.Gly1022= | |
| ENST00000587295.5:c.259C>A | ||
| ENST00000588098.1:c.43C>A | ||
| NM_000419.3:c.3066C>A , LRG_479t1:c.3066C>A | NP_000410.2:p.Gly1022= | |
| XM_011524749.1:c.2964C>A | XP_011523051.1:p.Gly988= | |
| XM_011524750.1:c.2949C>A | XP_011523052.1:p.Gly983= | |
| NM_000419.4:c.3066C>A | NP_000410.2:p.Gly1022= | |
| NM_000419.5:c.3066C>A MANE Select | NP_000410.2:p.Gly1022= |