Canonical Allele Identifier: CA2677060168
Gene: FOXC1 HGNC NCBI

Linked Data

gnomAD v4: 6-1610198-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610198G>A , CM000668.2:g.1610198G>A GRCh38
NC_000006.11:g.1610433G>A , CM000668.1:g.1610433G>A GRCh37
NC_000006.10:g.1555432G>A NCBI36
NG_009368.1:g.4753G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-248G>A MANE Select ENSP00000493906.1:n.-248G>A
ENST00000380874.3:c.-248G>A ENSP00000370256.2:n.-248G>A
NM_001453.3:c.-248G>A MANE Select NP_001444.2:n.-248G>A
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