Linked Data
MyVariant Identifiers:
chr15:g.80884030G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.80591689G>A , CM000677.2:g.80591689G>A | GRCh38 |
| NC_000015.9:g.80884030G>A , CM000677.1:g.80884030G>A | GRCh37 |
| NC_000015.8:g.78671085G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000303329.9:c.2040G>A MANE Select | ENSP00000307479.4:p.Gln680= | |
| ENST00000303329.8:c.2040G>A | ENSP00000307479.4:p.Gln680= | |
| ENST00000527771.5:c.2007G>A | ENSP00000453792.1:p.Gln669= | |
| ENST00000533983.5:c.2007G>A | ENSP00000453651.1:p.Gln669= | |
| ENST00000610490.4:c.*338G>A | ENSP00000483762.1:n.*338G>A | |
| ENST00000622346.4:c.2040G>A | ENSP00000479393.1:p.Gln680= | |
| NM_014862.3:c.2040G>A | NP_055677.3:p.Gln680= | |
| NM_014862.4:c.2040G>A MANE Select | NP_055677.3:p.Gln680= |