Canonical Allele Identifier: CA133389665
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1037208972
gnomAD v2: 6-1610985-A-G
gnomAD v3: 6-1610750-A-G
gnomAD v4: 6-1610750-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610750A>G , CM000668.2:g.1610750A>G GRCh38
NC_000006.11:g.1610985A>G , CM000668.1:g.1610985A>G GRCh37
NC_000006.10:g.1555984A>G NCBI36
NG_009368.1:g.5305A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.305A>G MANE Select ENSP00000493906.1:p.Asn102Ser
ENST00000380874.3:c.305A>G ENSP00000370256.2:p.Asn102Ser
NM_001453.2:c.305A>G NP_001444.2:p.Asn102Ser
NM_001453.3:c.305A>G MANE Select NP_001444.2:p.Asn102Ser