Canonical Allele Identifier: CA1605821868
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1609963G= , CM000668.2:g.1609963G= GRCh38
NC_000006.11:g.1610198G= , CM000668.1:g.1610198G= GRCh37
NC_000006.10:g.1555197G= NCBI36
NG_009368.1:g.4518G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-483G= MANE Select ENSP00000493906.1:n.-483G=
NM_001453.3:c.-483G= MANE Select NP_001444.2:n.-483G=