Canonical Allele Identifier: CA2677061174
Gene: FOXC1 HGNC NCBI

Linked Data

gnomAD v4: 6-1613031-A-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1613031A>G , CM000668.2:g.1613031A>G GRCh38
NC_000006.11:g.1613266A>G , CM000668.1:g.1613266A>G GRCh37
NC_000006.10:g.1558265A>G NCBI36
NG_009368.1:g.7586A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*924A>G MANE Select ENSP00000493906.1:n.*924A>G
ENST00000380874.3:c.*924A>G ENSP00000370256.2:n.*924A>G
NM_001453.2:c.2586A>G NP_001444.2:n.2586A>G
NM_001453.3:c.*924A>G MANE Select NP_001444.2:n.*924A>G
Search 100 bp 5'
Search 100 bp 3'