HGVS | Genome Assembly |
---|---|
NC_000004.12:g.176689730T>A , CM000666.2:g.176689730T>A | GRCh38 |
NC_000004.11:g.177610884T>A , CM000666.1:g.177610884T>A | GRCh37 |
NC_000004.10:g.177847878T>A | NCBI36 |
NG_034216.1:g.108016A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000618562.2:c.705-1803A>T (VEGFC) MANE Select | ENSP00000480043.1:n.705-1803A>T | |
ENST00000507638.1:n.404-75A>T (VEGFC) | ||
ENST00000618562.1:c.705-1803A>T (VEGFC) | ENSP00000480043.1:n.705-1803A>T | |
NM_005429.4:c.705-1803A>T (VEGFC) | NP_005420.1:n.705-1803A>T | |
XR_939498.1:n.260+9980T>A (HAFML) | ||
XR_939499.1:n.210-16173T>A (HAFML) | ||
XR_939498.2:n.347+9980T>A (HAFML) | ||
XR_939499.2:n.293-16173T>A (HAFML) | ||
NM_005429.5:c.705-1803A>T (VEGFC) MANE Select | NP_005420.1:n.705-1803A>T |