Canonical Allele Identifier: CA448393200
Gene: FOXC1 HGNC NCBI

Linked Data

gnomAD v4: 6-1610457-C-A
MyVariant Identifiers: chr6:g.1610692C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610457C>A , CM000668.2:g.1610457C>A GRCh38
NC_000006.11:g.1610692C>A , CM000668.1:g.1610692C>A GRCh37
NC_000006.10:g.1555691C>A NCBI36
NG_009368.1:g.5012C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.12C>A MANE Select ENSP00000493906.1:p.Arg4=
ENST00000380874.3:c.12C>A ENSP00000370256.2:p.Arg4=
NM_001453.2:c.12C>A NP_001444.2:p.Arg4=
NM_001453.3:c.12C>A MANE Select NP_001444.2:p.Arg4=