Canonical Allele Identifier: CA119641
Gene: FOXC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 8459
ClinVar RCV Id: RCV000008979
dbSNP Id: rs104893954

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610706C>G , CM000668.2:g.1610706C>G GRCh38
NC_000006.11:g.1610941C>G , CM000668.1:g.1610941C>G GRCh37
NC_000006.10:g.1555940C>G NCBI36
NG_009368.1:g.5261C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.261C>G MANE Select ENSP00000493906.1:p.Ile87Met
ENST00000380874.3:c.261C>G ENSP00000370256.2:p.Ile87Met
NM_001453.2:c.261C>G NP_001444.2:p.Ile87Met
NM_001453.3:c.261C>G MANE Select NP_001444.2:p.Ile87Met