Canonical Allele Identifier: CA1605821968
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610040T= , CM000668.2:g.1610040T= GRCh38
NC_000006.11:g.1610275T= , CM000668.1:g.1610275T= GRCh37
NC_000006.10:g.1555274T= NCBI36
NG_009368.1:g.4595T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-406T= MANE Select ENSP00000493906.1:n.-406T=
ENST00000380874.3:c.-406T= ENSP00000370256.2:n.-406T=
NM_001453.3:c.-406T= MANE Select NP_001444.2:n.-406T=