Canonical Allele Identifier: CA1085282757
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1762512730
gnomAD v3: 6-1610358-A-C
gnomAD v4: 6-1610358-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610358A>C , CM000668.2:g.1610358A>C GRCh38
NC_000006.11:g.1610593A>C , CM000668.1:g.1610593A>C GRCh37
NC_000006.10:g.1555592A>C NCBI36
NG_009368.1:g.4913A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.-88A>C MANE Select ENSP00000493906.1:n.-88A>C
ENST00000380874.3:c.-88A>C ENSP00000370256.2:n.-88A>C
NM_001453.3:c.-88A>C MANE Select NP_001444.2:n.-88A>C
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