Canonical Allele Identifier: CA358822951
Gene: VEGFC HGNC NCBI

Linked Data

gnomAD v4: 4-176727882-T-C
MyVariant Identifiers: chr4:g.177649036T>C (hg19) chr4:g.176727882T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.176727882T>C , CM000666.2:g.176727882T>C GRCh38
NC_000004.11:g.177649036T>C , CM000666.1:g.177649036T>C GRCh37
NC_000004.10:g.177886030T>C NCBI36
NG_034216.1:g.69864A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000618562.2:c.448A>G MANE Select ENSP00000480043.1:p.Thr150Ala
ENST00000507638.1:n.147A>G
ENST00000618562.1:c.448A>G ENSP00000480043.1:p.Thr150Ala
NM_005429.4:c.448A>G NP_005420.1:p.Thr150Ala
NM_005429.5:c.448A>G MANE Select NP_005420.1:p.Thr150Ala
Search 100 bp 5'
Search 100 bp 3'