Canonical Allele Identifier: CA2672740331

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.176687556A>C , CM000666.2:g.176687556A>C GRCh38
NC_000004.11:g.177608710A>C , CM000666.1:g.177608710A>C GRCh37
NC_000004.10:g.177845704A>C NCBI36
NG_034216.1:g.110190T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000618562.2:c.812-36T>G (VEGFC) MANE Select ENSP00000480043.1:n.812-36T>G
ENST00000618562.1:c.812-36T>G (VEGFC) ENSP00000480043.1:n.812-36T>G
NM_005429.4:c.812-36T>G (VEGFC) NP_005420.1:n.812-36T>G
XR_939498.1:n.260+7806A>C (HAFML)
XR_939499.1:n.209+17847A>C (HAFML)
XR_939498.2:n.347+7806A>C (HAFML)
XR_939499.2:n.292+17847A>C (HAFML)
NM_005429.5:c.812-36T>G (VEGFC) MANE Select NP_005420.1:n.812-36T>G