Canonical Allele Identifier: CA1605823839
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1762584301
gnomAD v4: 6-1613086-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1613086A>G , CM000668.2:g.1613086A>G GRCh38
NC_000006.11:g.1613321A>G , CM000668.1:g.1613321A>G GRCh37
NC_000006.10:g.1558320A>G NCBI36
NG_009368.1:g.7641A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*979A>G MANE Select ENSP00000493906.1:n.*979A>G
ENST00000380874.3:c.*979A>G ENSP00000370256.2:n.*979A>G
NM_001453.2:c.2641A>G NP_001444.2:n.2641A>G
NM_001453.3:c.*979A>G MANE Select NP_001444.2:n.*979A>G
Search 100 bp 5'
Search 100 bp 3'