Canonical Allele Identifier: CA1605823570
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1762575907
gnomAD v4: 6-1612539-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612539G>C , CM000668.2:g.1612539G>C GRCh38
NC_000006.11:g.1612774G>C , CM000668.1:g.1612774G>C GRCh37
NC_000006.10:g.1557773G>C NCBI36
NG_009368.1:g.7094G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*432G>C MANE Select ENSP00000493906.1:n.*432G>C
ENST00000380874.3:c.*432G>C ENSP00000370256.2:n.*432G>C
NM_001453.2:c.2094G>C NP_001444.2:n.2094G>C
NM_001453.3:c.*432G>C MANE Select NP_001444.2:n.*432G>C
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