Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.176687553C>T , CM000666.2:g.176687553C>T | GRCh38 |
| NC_000004.11:g.177608707C>T , CM000666.1:g.177608707C>T | GRCh37 |
| NC_000004.10:g.177845701C>T | NCBI36 |
| NG_034216.1:g.110193G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005429.5:c.812-33G>A (VEGFC) MANE Select | NP_005420.1:n.812-33G>A |
| ENST00000618562.2:c.812-33G>A (VEGFC) MANE Select | ENSP00000480043.1:n.812-33G>A |
| NM_005429.4:c.812-33G>A (VEGFC) | NP_005420.1:n.812-33G>A |
| ENST00000618562.1:c.812-33G>A (VEGFC) | ENSP00000480043.1:n.812-33G>A |
| XR_939498.1:n.260+7803C>T (HAFML) | |
| XR_939498.2:n.347+7803C>T (HAFML) | |
| XR_939499.1:n.209+17844C>T (HAFML) | |
| XR_939499.2:n.292+17844C>T (HAFML) |