Canonical Allele Identifier: CA2677060926
Gene: FOXC1 HGNC NCBI

Linked Data

gnomAD v4: 6-1612464-T-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612464T>A , CM000668.2:g.1612464T>A GRCh38
NC_000006.11:g.1612699T>A , CM000668.1:g.1612699T>A GRCh37
NC_000006.10:g.1557698T>A NCBI36
NG_009368.1:g.7019T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*357T>A MANE Select ENSP00000493906.1:n.*357T>A
ENST00000380874.3:c.*357T>A ENSP00000370256.2:n.*357T>A
NM_001453.2:c.2019T>A NP_001444.2:n.2019T>A
NM_001453.3:c.*357T>A MANE Select NP_001444.2:n.*357T>A
Search 100 bp 5'
Search 100 bp 3'