Canonical Allele Identifier: CA362558367
Gene: FOXC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3236698
ClinVar RCV Id: RCV004556158
MyVariant Identifiers: chr6:g.1610915C>A (hg19) chr6:g.1610680C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610680C>A , CM000668.2:g.1610680C>A GRCh38
NC_000006.11:g.1610915C>A , CM000668.1:g.1610915C>A GRCh37
NC_000006.10:g.1555914C>A NCBI36
NG_009368.1:g.5235C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.235C>A MANE Select ENSP00000493906.1:p.Pro79Thr
ENST00000380874.3:c.235C>A ENSP00000370256.2:p.Pro79Thr
NM_001453.2:c.235C>A NP_001444.2:p.Pro79Thr
NM_001453.3:c.235C>A MANE Select NP_001444.2:p.Pro79Thr
Search 100 bp 5'
Search 100 bp 3'