Canonical Allele Identifier: CA362558392
Gene: FOXC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1251979
ClinVar RCV Id: RCV001650517
dbSNP Id: rs376405759
MyVariant Identifiers: chr6:g.1610926C>A (hg19) chr6:g.1610691C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610691C>A , CM000668.2:g.1610691C>A GRCh38
NC_000006.11:g.1610926C>A , CM000668.1:g.1610926C>A GRCh37
NC_000006.10:g.1555925C>A NCBI36
NG_009368.1:g.5246C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.246C>A MANE Select ENSP00000493906.1:p.Ser82Arg
ENST00000380874.3:c.246C>A ENSP00000370256.2:p.Ser82Arg
NM_001453.2:c.246C>A NP_001444.2:p.Ser82Arg
NM_001453.3:c.246C>A MANE Select NP_001444.2:p.Ser82Arg
Search 100 bp 5'
Search 100 bp 3'