Canonical Allele Identifier: CA1605821879
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1609974A= , CM000668.2:g.1609974A= GRCh38
NC_000006.11:g.1610209A= , CM000668.1:g.1610209A= GRCh37
NC_000006.10:g.1555208A= NCBI36
NG_009368.1:g.4529A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-472A= MANE Select ENSP00000493906.1:n.-472A=
ENST00000380874.3:c.-472A= ENSP00000370256.2:n.-472A=
NM_001453.3:c.-472A= MANE Select NP_001444.2:n.-472A=