Canonical Allele Identifier: CA362558516
Gene: FOXC1 HGNC NCBI

Linked Data

gnomAD v4: 6-1610749-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610749A>G , CM000668.2:g.1610749A>G GRCh38
NC_000006.11:g.1610984A>G , CM000668.1:g.1610984A>G GRCh37
NC_000006.10:g.1555983A>G NCBI36
NG_009368.1:g.5304A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.304A>G MANE Select ENSP00000493906.1:p.Asn102Asp
ENST00000380874.3:c.304A>G ENSP00000370256.2:p.Asn102Asp
NM_001453.2:c.304A>G NP_001444.2:p.Asn102Asp
NM_001453.3:c.304A>G MANE Select NP_001444.2:p.Asn102Asp