Canonical Allele Identifier: CA2672740342

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.176687566G>T , CM000666.2:g.176687566G>T GRCh38
NC_000004.11:g.177608720G>T , CM000666.1:g.177608720G>T GRCh37
NC_000004.10:g.177845714G>T NCBI36
NG_034216.1:g.110180C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000618562.2:c.812-46C>A (VEGFC) MANE Select ENSP00000480043.1:n.812-46C>A
ENST00000618562.1:c.812-46C>A (VEGFC) ENSP00000480043.1:n.812-46C>A
NM_005429.4:c.812-46C>A (VEGFC) NP_005420.1:n.812-46C>A
XR_939498.1:n.260+7816G>T (HAFML)
XR_939499.1:n.209+17857G>T (HAFML)
XR_939498.2:n.347+7816G>T (HAFML)
XR_939499.2:n.292+17857G>T (HAFML)
NM_005429.5:c.812-46C>A (VEGFC) MANE Select NP_005420.1:n.812-46C>A