Canonical Allele Identifier: CA442494542
Gene: VEGFC HGNC NCBI

Linked Data

dbSNP Id: rs1269836397
gnomAD v4: 4-176727880-G-T
MyVariant Identifiers: chr4:g.177649034G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.176727880G>T , CM000666.2:g.176727880G>T GRCh38
NC_000004.11:g.177649034G>T , CM000666.1:g.177649034G>T GRCh37
NC_000004.10:g.177886028G>T NCBI36
NG_034216.1:g.69866C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000618562.2:c.450C>A MANE Select ENSP00000480043.1:p.Thr150=
ENST00000507638.1:n.149C>A
ENST00000618562.1:c.450C>A ENSP00000480043.1:p.Thr150=
NM_005429.4:c.450C>A NP_005420.1:p.Thr150=
NM_005429.5:c.450C>A MANE Select NP_005420.1:p.Thr150=
Search 100 bp 5'
Search 100 bp 3'