Canonical Allele Identifier: CA119637
Gene: FOXC1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 8455
ClinVar RCV Id: RCV000008973
dbSNP Id: rs104893952

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610512C>T , CM000668.2:g.1610512C>T GRCh38
NC_000006.11:g.1610747C>T , CM000668.1:g.1610747C>T GRCh37
NC_000006.10:g.1555746C>T NCBI36
NG_009368.1:g.5067C>T

Transcript Alleles

HGVS Amino-acid change
NM_001453.2:n.67C>T VV NP_001444.2:p.Gln23Ter
NM_001453.3:c.67C>T VV NP_001444.2:p.Gln23Ter
ENST00000380874.3:c.67C>T ENSP00000370256.2:p.Gln23Ter