Canonical Allele Identifier: CA565356163
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1433603777
gnomAD v2: 6-1610513-G-C
gnomAD v3: 6-1610278-G-C
gnomAD v4: 6-1610278-G-C
MyVariant Identifiers: chr6:g.1610513G>C (hg19) chr6:g.1610278G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610278G>C , CM000668.2:g.1610278G>C GRCh38
NC_000006.11:g.1610513G>C , CM000668.1:g.1610513G>C GRCh37
NC_000006.10:g.1555512G>C NCBI36
NG_009368.1:g.4833G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.-168G>C MANE Select ENSP00000493906.1:n.-168G>C
ENST00000380874.3:c.-168G>C ENSP00000370256.2:n.-168G>C
NM_001453.3:c.-168G>C MANE Select NP_001444.2:n.-168G>C
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