Canonical Allele Identifier: CA133392734
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1029465164
gnomAD v4: 6-1613064-C-A
MyVariant Identifiers: chr6:g.1613299C>A (hg19) chr6:g.1613064C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1613064C>A , CM000668.2:g.1613064C>A GRCh38
NC_000006.11:g.1613299C>A , CM000668.1:g.1613299C>A GRCh37
NC_000006.10:g.1558298C>A NCBI36
NG_009368.1:g.7619C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*957C>A MANE Select ENSP00000493906.1:n.*957C>A
ENST00000380874.3:c.*957C>A ENSP00000370256.2:n.*957C>A
NM_001453.2:c.2619C>A NP_001444.2:n.2619C>A
NM_001453.3:c.*957C>A MANE Select NP_001444.2:n.*957C>A
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