Canonical Allele Identifier: CA358822945
Gene: VEGFC HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.177649033A>C (hg19) chr4:g.176727879A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.176727879A>C , CM000666.2:g.176727879A>C GRCh38
NC_000004.11:g.177649033A>C , CM000666.1:g.177649033A>C GRCh37
NC_000004.10:g.177886027A>C NCBI36
NG_034216.1:g.69867T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000618562.2:c.451T>G MANE Select ENSP00000480043.1:p.Phe151Val
ENST00000507638.1:n.150T>G
ENST00000618562.1:c.451T>G ENSP00000480043.1:p.Phe151Val
NM_005429.4:c.451T>G NP_005420.1:p.Phe151Val
NM_005429.5:c.451T>G MANE Select NP_005420.1:p.Phe151Val
Search 100 bp 5'
Search 100 bp 3'