Canonical Allele Identifier: CA565018289
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1200473920
gnomAD v2: 6-1612990-C-T
gnomAD v3: 6-1612755-C-T
gnomAD v4: 6-1612755-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612755C>T , CM000668.2:g.1612755C>T GRCh38
NC_000006.11:g.1612990C>T , CM000668.1:g.1612990C>T GRCh37
NC_000006.10:g.1557989C>T NCBI36
NG_009368.1:g.7310C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.*648C>T MANE Select ENSP00000493906.1:n.*648C>T
ENST00000380874.3:c.*648C>T ENSP00000370256.2:n.*648C>T
NM_001453.2:c.2310C>T NP_001444.2:n.2310C>T
NM_001453.3:c.*648C>T MANE Select NP_001444.2:n.*648C>T