Canonical Allele Identifier: CA133388615
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1013874390
gnomAD v2: 6-1610263-C-A
gnomAD v3: 6-1610028-C-A
gnomAD v4: 6-1610028-C-A
MyVariant Identifiers: chr6:g.1610263C>A (hg19) chr6:g.1610028C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610028C>A , CM000668.2:g.1610028C>A GRCh38
NC_000006.11:g.1610263C>A , CM000668.1:g.1610263C>A GRCh37
NC_000006.10:g.1555262C>A NCBI36
NG_009368.1:g.4583C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-418C>A MANE Select ENSP00000493906.1:n.-418C>A
ENST00000380874.3:c.-418C>A ENSP00000370256.2:n.-418C>A
NM_001453.3:c.-418C>A MANE Select NP_001444.2:n.-418C>A
Search 100 bp 5'
Search 100 bp 3'