Canonical Allele Identifier: CA362558590
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1762522294
gnomAD v3: 6-1610782-C-A
gnomAD v4: 6-1610782-C-A
MyVariant Identifiers: chr6:g.1611017C>A (hg19) chr6:g.1610782C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610782C>A , CM000668.2:g.1610782C>A GRCh38
NC_000006.11:g.1611017C>A , CM000668.1:g.1611017C>A GRCh37
NC_000006.10:g.1556016C>A NCBI36
NG_009368.1:g.5337C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.337C>A MANE Select ENSP00000493906.1:p.Pro113Thr
ENST00000380874.3:c.337C>A ENSP00000370256.2:p.Pro113Thr
NM_001453.2:c.337C>A NP_001444.2:p.Pro113Thr
NM_001453.3:c.337C>A MANE Select NP_001444.2:p.Pro113Thr
Search 100 bp 5'
Search 100 bp 3'