Canonical Allele Identifier: CA1605821926
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610013C= , CM000668.2:g.1610013C= GRCh38
NC_000006.11:g.1610248C= , CM000668.1:g.1610248C= GRCh37
NC_000006.10:g.1555247C= NCBI36
NG_009368.1:g.4568C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-433C= MANE Select ENSP00000493906.1:n.-433C=
ENST00000380874.3:c.-433C= ENSP00000370256.2:n.-433C=
NM_001453.3:c.-433C= MANE Select NP_001444.2:n.-433C=