Linked Data
MyVariant Identifiers:
chr17:g.7405922G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7502603G>A , CM000679.2:g.7502603G>A | GRCh38 |
| NC_000017.10:g.7405922G>A , CM000679.1:g.7405922G>A | GRCh37 |
| NC_000017.9:g.7346646G>A | NCBI36 |
| NG_027747.1:g.23225G>A | |
| NG_027747.2:g.23225G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000617998.6:n.3057G>A | ||
| ENST00000674977.2:c.2658G>A | ENSP00000502190.2:p.Val886= | |
| ENST00000576114.1:n.124G>A | ||
| ENST00000617998.4:c.2658G>A | ENSP00000480158.1:p.Val886= | |
| ENST00000621442.4:c.2658G>A | ENSP00000483957.1:p.Val886= | |
| NM_000937.4:c.2658G>A | NP_000928.1:p.Val886= | |
| NM_000937.5:c.2658G>A MANE Select | NP_000928.1:p.Val886= |