Canonical Allele Identifier: CA1605823665
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1738850510

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612760T>C , CM000668.2:g.1612760T>C GRCh38
NC_000006.11:g.1612995T>C , CM000668.1:g.1612995T>C GRCh37
NC_000006.10:g.1557994T>C NCBI36
NG_009368.1:g.7315T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.*653T>C MANE Select ENSP00000493906.1:n.*653T>C
ENST00000380874.3:c.*653T>C ENSP00000370256.2:n.*653T>C
NM_001453.2:c.2315T>C NP_001444.2:n.2315T>C
NM_001453.3:c.*653T>C MANE Select NP_001444.2:n.*653T>C