Linked Data
MyVariant Identifiers:
chr7:g.107341560C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.107701115C>G , CM000669.2:g.107701115C>G | GRCh38 |
| NC_000007.13:g.107341560C>G , CM000669.1:g.107341560C>G | GRCh37 |
| NC_000007.12:g.107128796C>G | NCBI36 |
| NG_008489.1:g.45481C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000644269.2:c.1722C>G MANE Select | ENSP00000494017.1:p.Ala574= | |
| ENST00000644846.1:c.433C>G | ||
| ENST00000265715.7:c.1722C>G | ENSP00000265715.3:p.Ala574= | |
| ENST00000480841.5:n.571C>G | ||
| ENST00000492030.2:n.91-712C>G | ||
| NM_000441.1:c.1722C>G | NP_000432.1:p.Ala574= | |
| XM_005250425.1:c.1722C>G | XP_005250482.1:p.Ala574= | |
| XM_005250425.2:c.1722C>G | XP_005250482.1:p.Ala574= | |
| XM_017012318.1:c.1644C>G | XP_016867807.1:p.Ala548= | |
| NM_000441.2:c.1722C>G MANE Select | NP_000432.1:p.Ala574= |