Canonical Allele Identifier: CA1605821819
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1609915G= , CM000668.2:g.1609915G= GRCh38
NC_000006.11:g.1610150G= , CM000668.1:g.1610150G= GRCh37
NC_000006.10:g.1555149G= NCBI36
NG_009368.1:g.4470G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-531G= MANE Select ENSP00000493906.1:n.-531G=
NM_001453.3:c.-531G= MANE Select NP_001444.2:n.-531G=