Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.176685497T>C , CM000666.2:g.176685497T>C | GRCh38 |
| NC_000004.11:g.177606651T>C , CM000666.1:g.177606651T>C | GRCh37 |
| NC_000004.10:g.177843645T>C | NCBI36 |
| NG_034216.1:g.112249A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005429.5:c.1146-1457A>G (VEGFC) MANE Select | NP_005420.1:n.1146-1457A>G |
| ENST00000618562.2:c.1146-1457A>G (VEGFC) MANE Select | ENSP00000480043.1:n.1146-1457A>G |
| NM_005429.4:c.1146-1457A>G (VEGFC) | NP_005420.1:n.1146-1457A>G |
| ENST00000618562.1:c.1146-1457A>G (VEGFC) | ENSP00000480043.1:n.1146-1457A>G |
| XR_939498.1:n.260+5747T>C (HAFML) | |
| XR_939498.2:n.347+5747T>C (HAFML) | |
| XR_939499.1:n.209+15788T>C (HAFML) | |
| XR_939499.2:n.292+15788T>C (HAFML) |