Canonical Allele Identifier: CA821645412
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1218039696
gnomAD v3: 6-1610012-G-A
gnomAD v4: 6-1610012-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610012G>A , CM000668.2:g.1610012G>A GRCh38
NC_000006.11:g.1610247G>A , CM000668.1:g.1610247G>A GRCh37
NC_000006.10:g.1555246G>A NCBI36
NG_009368.1:g.4567G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-434G>A MANE Select ENSP00000493906.1:n.-434G>A
ENST00000380874.3:c.-434G>A ENSP00000370256.2:n.-434G>A
NM_001453.3:c.-434G>A MANE Select NP_001444.2:n.-434G>A