Canonical Allele Identifier: CA1605822265
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1762513672
gnomAD v4: 6-1610404-TG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610410del , CM000668.2:g.1610410del GRCh38
NC_000006.11:g.1610645del , CM000668.1:g.1610645del GRCh37
NC_000006.10:g.1555644del NCBI36
NG_009368.1:g.4965del

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-36del MANE Select ENSP00000493906.1:n.-36del
ENST00000380874.3:c.-36del ENSP00000370256.2:n.-36del
NM_001453.3:c.-36del MANE Select NP_001444.2:n.-36del
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Search 100 bp 3'