Canonical Allele Identifier: CA1605823528
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1762574839
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612478dup , CM000668.2:g.1612478dup GRCh38
NC_000006.11:g.1612713dup , CM000668.1:g.1612713dup GRCh37
NC_000006.10:g.1557712dup NCBI36
NG_009368.1:g.7033dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*371dup MANE Select ENSP00000493906.1:n.*371dup
ENST00000380874.3:c.*371dup ENSP00000370256.2:n.*371dup
NM_001453.2:c.2033dup NP_001444.2:n.2033dup
NM_001453.3:c.*371dup MANE Select NP_001444.2:n.*371dup
Search 100 bp 5'
Search 100 bp 3'