Canonical Allele Identifier: CA1605822368
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610552G= , CM000668.2:g.1610552G= GRCh38
NC_000006.11:g.1610787G= , CM000668.1:g.1610787G= GRCh37
NC_000006.10:g.1555786G= NCBI36
NG_009368.1:g.5107G=

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.107G= MANE Select ENSP00000493906.1:p.Gly36=
ENST00000380874.3:c.107G= ENSP00000370256.2:p.Gly36=
NM_001453.2:c.107G= NP_001444.2:p.Gly36=
NM_001453.3:c.107G= MANE Select NP_001444.2:p.Gly36=