Canonical Allele Identifier: CA1605821886
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1609982T= , CM000668.2:g.1609982T= GRCh38
NC_000006.11:g.1610217T= , CM000668.1:g.1610217T= GRCh37
NC_000006.10:g.1555216T= NCBI36
NG_009368.1:g.4537T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-464T= MANE Select ENSP00000493906.1:n.-464T=
ENST00000380874.3:c.-464T= ENSP00000370256.2:n.-464T=
NM_001453.3:c.-464T= MANE Select NP_001444.2:n.-464T=