Canonical Allele Identifier: CA1605821854
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1762499740
gnomAD v4: 6-1609947-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1609947C>A , CM000668.2:g.1609947C>A GRCh38
NC_000006.11:g.1610182C>A , CM000668.1:g.1610182C>A GRCh37
NC_000006.10:g.1555181C>A NCBI36
NG_009368.1:g.4502C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-499C>A MANE Select ENSP00000493906.1:n.-499C>A
NM_001453.3:c.-499C>A MANE Select NP_001444.2:n.-499C>A