Linked Data
MyVariant Identifiers:
chr1:g.109806978C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.109264356C>A , CM000663.2:g.109264356C>A | GRCh38 |
| NC_000001.10:g.109806978C>A , CM000663.1:g.109806978C>A | GRCh37 |
| NC_000001.9:g.109608501C>A | NCBI36 |
| NG_052669.1:g.19652C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000271332.4:c.5280C>A MANE Select | ENSP00000271332.3:p.Gly1760= | |
| ENST00000271332.3:c.5280C>A | ENSP00000271332.3:p.Gly1760= | |
| NM_001408.2:c.5280C>A | NP_001399.1:p.Gly1760= | |
| XM_005270580.3:c.5280C>A | XP_005270637.1:p.Gly1760= | |
| NM_001408.3:c.5280C>A MANE Select | NP_001399.1:p.Gly1760= |