HGVS | Genome Assembly |
---|---|
NC_000004.12:g.176687464T>C , CM000666.2:g.176687464T>C | GRCh38 |
NC_000004.11:g.177608618T>C , CM000666.1:g.177608618T>C | GRCh37 |
NC_000004.10:g.177845612T>C | NCBI36 |
NG_034216.1:g.110282A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000618562.2:c.868A>G (VEGFC) MANE Select | ENSP00000480043.1:p.Thr290Ala | |
ENST00000618562.1:c.868A>G (VEGFC) | ENSP00000480043.1:p.Thr290Ala | |
NM_005429.4:c.868A>G (VEGFC) | NP_005420.1:p.Thr290Ala | |
XR_939498.1:n.260+7714T>C (HAFML) | ||
XR_939499.1:n.209+17755T>C (HAFML) | ||
XR_939498.2:n.347+7714T>C (HAFML) | ||
XR_939499.2:n.292+17755T>C (HAFML) | ||
NM_005429.5:c.868A>G (VEGFC) MANE Select | NP_005420.1:p.Thr290Ala |