Canonical Allele Identifier: CA2590755705
Gene: FOXC1 HGNC NCBI

Linked Data

gnomAD v3: 6-1609999-A-C
gnomAD v4: 6-1609999-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1609999A>C , CM000668.2:g.1609999A>C GRCh38
NC_000006.11:g.1610234A>C , CM000668.1:g.1610234A>C GRCh37
NC_000006.10:g.1555233A>C NCBI36
NG_009368.1:g.4554A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-447A>C MANE Select ENSP00000493906.1:n.-447A>C
ENST00000380874.3:c.-447A>C ENSP00000370256.2:n.-447A>C
NM_001453.3:c.-447A>C MANE Select NP_001444.2:n.-447A>C