Canonical Allele Identifier: CA2677060010
Gene: FOXC1 HGNC NCBI

Linked Data

gnomAD v4: 6-1609937-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1609937C>A , CM000668.2:g.1609937C>A GRCh38
NC_000006.11:g.1610172C>A , CM000668.1:g.1610172C>A GRCh37
NC_000006.10:g.1555171C>A NCBI36
NG_009368.1:g.4492C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-509C>A MANE Select ENSP00000493906.1:n.-509C>A
NM_001453.3:c.-509C>A MANE Select NP_001444.2:n.-509C>A