Canonical Allele Identifier: CA442537678

Linked Data

MyVariant Identifiers: chr4:g.177608616G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.176687462G>T , CM000666.2:g.176687462G>T GRCh38
NC_000004.11:g.177608616G>T , CM000666.1:g.177608616G>T GRCh37
NC_000004.10:g.177845610G>T NCBI36
NG_034216.1:g.110284C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000618562.2:c.870C>A (VEGFC) MANE Select ENSP00000480043.1:p.Thr290=
ENST00000618562.1:c.870C>A (VEGFC) ENSP00000480043.1:p.Thr290=
NM_005429.4:c.870C>A (VEGFC) NP_005420.1:p.Thr290=
XR_939498.1:n.260+7712G>T (HAFML)
XR_939499.1:n.209+17753G>T (HAFML)
XR_939498.2:n.347+7712G>T (HAFML)
XR_939499.2:n.292+17753G>T (HAFML)
NM_005429.5:c.870C>A (VEGFC) MANE Select NP_005420.1:p.Thr290=