Canonical Allele Identifier: CA1085282596
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1433143817
gnomAD v3: 6-1610092-A-G
gnomAD v4: 6-1610092-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610092A>G , CM000668.2:g.1610092A>G GRCh38
NC_000006.11:g.1610327A>G , CM000668.1:g.1610327A>G GRCh37
NC_000006.10:g.1555326A>G NCBI36
NG_009368.1:g.4647A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-354A>G MANE Select ENSP00000493906.1:n.-354A>G
ENST00000380874.3:c.-354A>G ENSP00000370256.2:n.-354A>G
NM_001453.3:c.-354A>G MANE Select NP_001444.2:n.-354A>G