Canonical Allele Identifier: CA1605821848
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1609940A= , CM000668.2:g.1609940A= GRCh38
NC_000006.11:g.1610175A= , CM000668.1:g.1610175A= GRCh37
NC_000006.10:g.1555174A= NCBI36
NG_009368.1:g.4495A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-506A= MANE Select ENSP00000493906.1:n.-506A=
NM_001453.3:c.-506A= MANE Select NP_001444.2:n.-506A=