Canonical Allele Identifier: CA565018296
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1478976089
gnomAD v2: 6-1613104-A-C
gnomAD v3: 6-1612869-A-C
gnomAD v4: 6-1612869-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612869A>C , CM000668.2:g.1612869A>C GRCh38
NC_000006.11:g.1613104A>C , CM000668.1:g.1613104A>C GRCh37
NC_000006.10:g.1558103A>C NCBI36
NG_009368.1:g.7424A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.*762A>C MANE Select ENSP00000493906.1:n.*762A>C
ENST00000380874.3:c.*762A>C ENSP00000370256.2:n.*762A>C
NM_001453.2:c.2424A>C NP_001444.2:n.2424A>C
NM_001453.3:c.*762A>C MANE Select NP_001444.2:n.*762A>C