Canonical Allele Identifier: CA3614753
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs9502980
ExAC: 6:1611089 G / A
gnomAD v2: 6-1611089-G-A
gnomAD v3: 6-1610854-G-A
gnomAD v4: 6-1610854-G-A
MyVariant Identifiers: chr6:g.1611089G>A (hg19) chr6:g.1610854G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610854G>A , CM000668.2:g.1610854G>A GRCh38
NC_000006.11:g.1611089G>A , CM000668.1:g.1611089G>A GRCh37
NC_000006.10:g.1556088G>A NCBI36
NG_009368.1:g.5409G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.409G>A MANE Select ENSP00000493906.1:p.Val137Ile
ENST00000380874.3:c.409G>A ENSP00000370256.2:p.Val137Ile
NM_001453.2:c.409G>A NP_001444.2:p.Val137Ile
NM_001453.3:c.409G>A MANE Select NP_001444.2:p.Val137Ile
Search 100 bp 5'
Search 100 bp 3'