Canonical Allele Identifier: CA1605821828
Gene: FOXC1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1609923G= , CM000668.2:g.1609923G= GRCh38
NC_000006.11:g.1610158G= , CM000668.1:g.1610158G= GRCh37
NC_000006.10:g.1555157G= NCBI36
NG_009368.1:g.4478G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-523G= MANE Select ENSP00000493906.1:n.-523G=
NM_001453.3:c.-523G= MANE Select NP_001444.2:n.-523G=
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