Canonical Allele Identifier: CA1605822398
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610600A= , CM000668.2:g.1610600A= GRCh38
NC_000006.11:g.1610835A= , CM000668.1:g.1610835A= GRCh37
NC_000006.10:g.1555834A= NCBI36
NG_009368.1:g.5155A=

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.155A= MANE Select ENSP00000493906.1:p.His52=
ENST00000380874.3:c.155A= ENSP00000370256.2:p.His52=
NM_001453.2:c.155A= NP_001444.2:p.His52=
NM_001453.3:c.155A= MANE Select NP_001444.2:p.His52=