Canonical Allele Identifier: CA2578237965

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.176687577G>C , CM000666.2:g.176687577G>C GRCh38
NC_000004.11:g.177608731G>C , CM000666.1:g.177608731G>C GRCh37
NC_000004.10:g.177845725G>C NCBI36
NG_034216.1:g.110169C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000618562.2:c.812-57C>G (VEGFC) MANE Select ENSP00000480043.1:n.812-57C>G
ENST00000618562.1:c.812-57C>G (VEGFC) ENSP00000480043.1:n.812-57C>G
NM_005429.4:c.812-57C>G (VEGFC) NP_005420.1:n.812-57C>G
XR_939498.1:n.260+7827G>C (HAFML)
XR_939499.1:n.209+17868G>C (HAFML)
XR_939498.2:n.347+7827G>C (HAFML)
XR_939499.2:n.292+17868G>C (HAFML)
NM_005429.5:c.812-57C>G (VEGFC) MANE Select NP_005420.1:n.812-57C>G