Canonical Allele Identifier: CA1605821955
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1762503169
gnomAD v3: 6-1610028-C-CCG
gnomAD v4: 6-1610028-C-CCG
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610030_1610031dup , CM000668.2:g.1610030_1610031dup GRCh38
NC_000006.11:g.1610265_1610266dup , CM000668.1:g.1610265_1610266dup GRCh37
NC_000006.10:g.1555264_1555265dup NCBI36
NG_009368.1:g.4585_4586dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-416_-415dup MANE Select ENSP00000493906.1:n.-416_-415dup
ENST00000380874.3:c.-416_-415dup ENSP00000370256.2:n.-416_-415dup
NM_001453.3:c.-416_-415dup MANE Select NP_001444.2:n.-416_-415dup
Search 100 bp 5'
Search 100 bp 3'