Canonical Allele Identifier: CA133388481
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs894270015
gnomAD v3: 6-1609943-C-T
gnomAD v4: 6-1609943-C-T
MyVariant Identifiers: chr6:g.1610178C>T (hg19) chr6:g.1609943C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1609943C>T , CM000668.2:g.1609943C>T GRCh38
NC_000006.11:g.1610178C>T , CM000668.1:g.1610178C>T GRCh37
NC_000006.10:g.1555177C>T NCBI36
NG_009368.1:g.4498C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-503C>T MANE Select ENSP00000493906.1:n.-503C>T
NM_001453.3:c.-503C>T MANE Select NP_001444.2:n.-503C>T
Search 100 bp 5'
Search 100 bp 3'