Canonical Allele Identifier: CA821650204
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1171595558
gnomAD v3: 6-1612970-A-G
gnomAD v4: 6-1612970-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612970A>G , CM000668.2:g.1612970A>G GRCh38
NC_000006.11:g.1613205A>G , CM000668.1:g.1613205A>G GRCh37
NC_000006.10:g.1558204A>G NCBI36
NG_009368.1:g.7525A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*863A>G MANE Select ENSP00000493906.1:n.*863A>G
ENST00000380874.3:c.*863A>G ENSP00000370256.2:n.*863A>G
NM_001453.2:c.2525A>G NP_001444.2:n.2525A>G
NM_001453.3:c.*863A>G MANE Select NP_001444.2:n.*863A>G