Linked Data
MyVariant Identifiers:
chr3:g.129251459T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.129532616T>G , CM000665.2:g.129532616T>G | GRCh38 |
| NC_000003.11:g.129251459T>G , CM000665.1:g.129251459T>G | GRCh37 |
| NC_000003.10:g.130734149T>G | NCBI36 |
| NG_009115.1:g.8978T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000296271.4:c.780T>G MANE Select | ENSP00000296271.3:p.Ala260= | |
| ENST00000296271.3:c.780T>G | ENSP00000296271.3:p.Ala260= | |
| NM_000539.3:c.780T>G MANE Select | NP_000530.1:p.Ala260= |