Canonical Allele Identifier: CA1085281977
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1762499007
gnomAD v3: 6-1609916-C-CTCTT
gnomAD v4: 6-1609916-C-CTCTT
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1609918_1609919insTTTC , CM000668.2:g.1609918_1609919insTTTC GRCh38
NC_000006.11:g.1610153_1610154insTTTC , CM000668.1:g.1610153_1610154insTTTC GRCh37
NC_000006.10:g.1555152_1555153insTTTC NCBI36
NG_009368.1:g.4473_4474insTTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-528_-527insTTTC MANE Select ENSP00000493906.1:n.-528_-527insTTTC
NM_001453.3:c.-528_-527insTTTC MANE Select NP_001444.2:n.-528_-527insTTTC
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