Canonical Allele Identifier: CA1605821849
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1609942G= , CM000668.2:g.1609942G= GRCh38
NC_000006.11:g.1610177G= , CM000668.1:g.1610177G= GRCh37
NC_000006.10:g.1555176G= NCBI36
NG_009368.1:g.4497G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-504G= MANE Select ENSP00000493906.1:n.-504G=
NM_001453.3:c.-504G= MANE Select NP_001444.2:n.-504G=