Canonical Allele Identifier: CA565018228
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1303575386
gnomAD v2: 6-1610356-T-C
gnomAD v3: 6-1610121-T-C
gnomAD v4: 6-1610121-T-C
MyVariant Identifiers: chr6:g.1610356T>C (hg19) chr6:g.1610121T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610121T>C , CM000668.2:g.1610121T>C GRCh38
NC_000006.11:g.1610356T>C , CM000668.1:g.1610356T>C GRCh37
NC_000006.10:g.1555355T>C NCBI36
NG_009368.1:g.4676T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-325T>C MANE Select ENSP00000493906.1:n.-325T>C
ENST00000380874.3:c.-325T>C ENSP00000370256.2:n.-325T>C
NM_001453.3:c.-325T>C MANE Select NP_001444.2:n.-325T>C
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