Canonical Allele Identifier: CA2677061101
Gene: FOXC1 HGNC NCBI

Linked Data

gnomAD v4: 6-1612877-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612877T>G , CM000668.2:g.1612877T>G GRCh38
NC_000006.11:g.1613112T>G , CM000668.1:g.1613112T>G GRCh37
NC_000006.10:g.1558111T>G NCBI36
NG_009368.1:g.7432T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.*770T>G MANE Select ENSP00000493906.1:n.*770T>G
ENST00000380874.3:c.*770T>G ENSP00000370256.2:n.*770T>G
NM_001453.2:c.2432T>G NP_001444.2:n.2432T>G
NM_001453.3:c.*770T>G MANE Select NP_001444.2:n.*770T>G