Canonical Allele Identifier: CA821645622
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1377095657
gnomAD v3: 6-1610275-C-T
gnomAD v4: 6-1610275-C-T
MyVariant Identifiers: chr6:g.1610510C>T (hg19) chr6:g.1610275C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610275C>T , CM000668.2:g.1610275C>T GRCh38
NC_000006.11:g.1610510C>T , CM000668.1:g.1610510C>T GRCh37
NC_000006.10:g.1555509C>T NCBI36
NG_009368.1:g.4830C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.-171C>T MANE Select ENSP00000493906.1:n.-171C>T
ENST00000380874.3:c.-171C>T ENSP00000370256.2:n.-171C>T
NM_001453.3:c.-171C>T MANE Select NP_001444.2:n.-171C>T
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