Canonical Allele Identifier: CA650480754
Gene: FOXC1 HGNC NCBI

Linked Data

gnomAD v4: 6-1612487-C-T
COSMIC: COSN7697022
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612487C>T , CM000668.2:g.1612487C>T GRCh38
NC_000006.11:g.1612722C>T , CM000668.1:g.1612722C>T GRCh37
NC_000006.10:g.1557721C>T NCBI36
NG_009368.1:g.7042C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*380C>T MANE Select ENSP00000493906.1:n.*380C>T
ENST00000380874.3:c.*380C>T ENSP00000370256.2:n.*380C>T
NM_001453.2:c.2042C>T NP_001444.2:n.2042C>T
NM_001453.3:c.*380C>T MANE Select NP_001444.2:n.*380C>T
Search 100 bp 5'
Search 100 bp 3'