Canonical Allele Identifier: CA1605821880
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1609976A= , CM000668.2:g.1609976A= GRCh38
NC_000006.11:g.1610211A= , CM000668.1:g.1610211A= GRCh37
NC_000006.10:g.1555210A= NCBI36
NG_009368.1:g.4531A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-470A= MANE Select ENSP00000493906.1:n.-470A=
ENST00000380874.3:c.-470A= ENSP00000370256.2:n.-470A=
NM_001453.3:c.-470A= MANE Select NP_001444.2:n.-470A=