Linked Data
MyVariant Identifiers:
chr22:g.28146972C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.27750984C>A , CM000684.2:g.27750984C>A | GRCh38 |
| NC_000022.10:g.28146972C>A , CM000684.1:g.28146972C>A | GRCh37 |
| NC_000022.9:g.26476972C>A | NCBI36 |
| NG_023258.1:g.55515G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000703102.1:n.419G>T | ||
| ENST00000302326.5:c.3894G>T MANE Select | ENSP00000304956.4:p.Val1298= | |
| ENST00000302326.4:c.3894G>T | ENSP00000304956.4:p.Val1298= | |
| ENST00000424656.1:c.247G>T | ||
| ENST00000497225.1:n.250G>T | ||
| NM_002430.2:c.3894G>T | NP_002421.3:p.Val1298= | |
| NM_002430.3:c.3894G>T MANE Select | NP_002421.3:p.Val1298= |