Canonical Allele Identifier: CA2677060954
Gene: FOXC1 HGNC NCBI

Linked Data

gnomAD v4: 6-1612488-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612488T>A , CM000668.2:g.1612488T>A GRCh38
NC_000006.11:g.1612723T>A , CM000668.1:g.1612723T>A GRCh37
NC_000006.10:g.1557722T>A NCBI36
NG_009368.1:g.7043T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*381T>A MANE Select ENSP00000493906.1:n.*381T>A
ENST00000380874.3:c.*381T>A ENSP00000370256.2:n.*381T>A
NM_001453.2:c.2043T>A NP_001444.2:n.2043T>A
NM_001453.3:c.*381T>A MANE Select NP_001444.2:n.*381T>A
Search 100 bp 5'
Search 100 bp 3'