Canonical Allele Identifier: CA821650331
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1276986857

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1613249T>A , CM000668.2:g.1613249T>A GRCh38
NC_000006.11:g.1613484T>A , CM000668.1:g.1613484T>A GRCh37
NC_000006.10:g.1558483T>A NCBI36
NG_009368.1:g.7804T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*1142T>A MANE Select ENSP00000493906.1:n.*1142T>A
ENST00000380874.3:c.*1142T>A ENSP00000370256.2:n.*1142T>A
NM_001453.2:c.2804T>A NP_001444.2:n.2804T>A
NM_001453.3:c.*1142T>A MANE Select NP_001444.2:n.*1142T>A