Canonical Allele Identifier: CA1605823536
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1756043723
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612485T>G , CM000668.2:g.1612485T>G GRCh38
NC_000006.11:g.1612720T>G , CM000668.1:g.1612720T>G GRCh37
NC_000006.10:g.1557719T>G NCBI36
NG_009368.1:g.7040T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*378T>G MANE Select ENSP00000493906.1:n.*378T>G
ENST00000380874.3:c.*378T>G ENSP00000370256.2:n.*378T>G
NM_001453.2:c.2040T>G NP_001444.2:n.2040T>G
NM_001453.3:c.*378T>G MANE Select NP_001444.2:n.*378T>G
Search 100 bp 5'
Search 100 bp 3'