Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.86567654C>G , CM000678.2:g.86567654C>G | GRCh38 |
| NC_000016.9:g.86601260C>G , CM000678.1:g.86601260C>G | GRCh37 |
| NC_000016.8:g.85158761C>G | NCBI36 |
| NG_012025.1:g.5404C>G | |
| NG_012025.2:g.5826C>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005251.3:c.319C>G (FOXC2) MANE Select | NP_005242.1:p.Pro107Ala |
| ENST00000649859.1:c.319C>G (FOXC2) MANE Select | ENSP00000497759.1:p.Pro107Ala |
| NM_005251.2:c.319C>G (FOXC2) | NP_005242.1:p.Pro107Ala |
| NR_125795.1:n.108G>C (FOXC2-AS1) | |
| ENST00000320354.5:c.319C>G (FOXC2) | ENSP00000326371.4:p.Pro107Ala |