Canonical Allele Identifier: CA1605821938
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610020C= , CM000668.2:g.1610020C= GRCh38
NC_000006.11:g.1610255C= , CM000668.1:g.1610255C= GRCh37
NC_000006.10:g.1555254C= NCBI36
NG_009368.1:g.4575C=

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.-426C= MANE Select ENSP00000493906.1:n.-426C=
ENST00000380874.3:c.-426C= ENSP00000370256.2:n.-426C=
NM_001453.3:c.-426C= MANE Select NP_001444.2:n.-426C=