Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.176702723C= , CM000666.2:g.176702723C= | GRCh38 |
| NC_000004.11:g.177623877C= , CM000666.1:g.177623877C= | GRCh37 |
| NC_000004.10:g.177860871C= | NCBI36 |
| NG_034216.1:g.95023G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000618562.2:c.704+8776G= (VEGFC) MANE Select | ENSP00000480043.1:n.704+8776G= | |
| ENST00000507638.1:n.403+8776G= (VEGFC) | ||
| ENST00000618562.1:c.704+8776G= (VEGFC) | ENSP00000480043.1:n.704+8776G= | |
| NM_005429.4:c.704+8776G= (VEGFC) | NP_005420.1:n.704+8776G= | |
| XR_939498.1:n.261-3180C= (HAFML) | ||
| XR_939499.1:n.210-3180C= (HAFML) | ||
| XR_939498.2:n.348-3180C= (HAFML) | ||
| XR_939499.2:n.293-3180C= (HAFML) | ||
| NM_005429.5:c.704+8776G= (VEGFC) MANE Select | NP_005420.1:n.704+8776G= |