Linked Data
MyVariant Identifiers:
chr3:g.129249783C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.129530940C>A , CM000665.2:g.129530940C>A | GRCh38 |
| NC_000003.11:g.129249783C>A , CM000665.1:g.129249783C>A | GRCh37 |
| NC_000003.10:g.130732473C>A | NCBI36 |
| NG_009115.1:g.7302C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296271.4:c.426C>A MANE Select | ENSP00000296271.3:p.Pro142= | |
| ENST00000296271.3:c.426C>A | ENSP00000296271.3:p.Pro142= | |
| NM_000539.3:c.426C>A MANE Select | NP_000530.1:p.Pro142= |