Canonical Allele Identifier: CA358822935
Gene: VEGFC HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.177649029A>G (hg19) chr4:g.176727875A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.176727875A>G , CM000666.2:g.176727875A>G GRCh38
NC_000004.11:g.177649029A>G , CM000666.1:g.177649029A>G GRCh37
NC_000004.10:g.177886023A>G NCBI36
NG_034216.1:g.69871T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000618562.2:c.455T>C MANE Select ENSP00000480043.1:p.Phe152Ser
ENST00000507638.1:n.154T>C
ENST00000618562.1:c.455T>C ENSP00000480043.1:p.Phe152Ser
NM_005429.4:c.455T>C NP_005420.1:p.Phe152Ser
NM_005429.5:c.455T>C MANE Select NP_005420.1:p.Phe152Ser
Search 100 bp 5'
Search 100 bp 3'