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