Canonical Allele Identifier: CA821650081
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1252687696
MyVariant Identifiers: chr6:g.1612956T>C (hg19) chr6:g.1612721T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612721T>C , CM000668.2:g.1612721T>C GRCh38
NC_000006.11:g.1612956T>C , CM000668.1:g.1612956T>C GRCh37
NC_000006.10:g.1557955T>C NCBI36
NG_009368.1:g.7276T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*614T>C MANE Select ENSP00000493906.1:n.*614T>C
ENST00000380874.3:c.*614T>C ENSP00000370256.2:n.*614T>C
NM_001453.2:c.2276T>C NP_001444.2:n.2276T>C
NM_001453.3:c.*614T>C MANE Select NP_001444.2:n.*614T>C
Search 100 bp 5'
Search 100 bp 3'