Canonical Allele Identifier: CA1605823620
Gene: FOXC1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612680G= , CM000668.2:g.1612680G= GRCh38
NC_000006.11:g.1612915G= , CM000668.1:g.1612915G= GRCh37
NC_000006.10:g.1557914G= NCBI36
NG_009368.1:g.7235G=

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.*573G= MANE Select ENSP00000493906.1:n.*573G=
ENST00000380874.3:c.*573G= ENSP00000370256.2:n.*573G=
NM_001453.2:c.2235G= NP_001444.2:n.2235G=
NM_001453.3:c.*573G= MANE Select NP_001444.2:n.*573G=
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