Canonical Allele Identifier: CA442537677

Linked Data

MyVariant Identifiers: chr4:g.177608613A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.176687459A>G , CM000666.2:g.176687459A>G GRCh38
NC_000004.11:g.177608613A>G , CM000666.1:g.177608613A>G GRCh37
NC_000004.10:g.177845607A>G NCBI36
NG_034216.1:g.110287T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000618562.2:c.873T>C (VEGFC) MANE Select ENSP00000480043.1:p.Cys291=
ENST00000618562.1:c.873T>C (VEGFC) ENSP00000480043.1:p.Cys291=
NM_005429.4:c.873T>C (VEGFC) NP_005420.1:p.Cys291=
XR_939498.1:n.260+7709A>G (HAFML)
XR_939499.1:n.209+17750A>G (HAFML)
XR_939498.2:n.347+7709A>G (HAFML)
XR_939499.2:n.292+17750A>G (HAFML)
NM_005429.5:c.873T>C (VEGFC) MANE Select NP_005420.1:p.Cys291=