Canonical Allele Identifier: CA821645507
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1388710051
gnomAD v3: 6-1610090-G-A
gnomAD v4: 6-1610090-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610090G>A , CM000668.2:g.1610090G>A GRCh38
NC_000006.11:g.1610325G>A , CM000668.1:g.1610325G>A GRCh37
NC_000006.10:g.1555324G>A NCBI36
NG_009368.1:g.4645G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-356G>A MANE Select ENSP00000493906.1:n.-356G>A
ENST00000380874.3:c.-356G>A ENSP00000370256.2:n.-356G>A
NM_001453.3:c.-356G>A MANE Select NP_001444.2:n.-356G>A