Canonical Allele Identifier: CA133392408
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs528961345
gnomAD v2: 6-1612981-T-G
gnomAD v3: 6-1612746-T-G
gnomAD v4: 6-1612746-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612746T>G , CM000668.2:g.1612746T>G GRCh38
NC_000006.11:g.1612981T>G , CM000668.1:g.1612981T>G GRCh37
NC_000006.10:g.1557980T>G NCBI36
NG_009368.1:g.7301T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.*639T>G MANE Select ENSP00000493906.1:n.*639T>G
ENST00000380874.3:c.*639T>G ENSP00000370256.2:n.*639T>G
NM_001453.2:c.2301T>G NP_001444.2:n.2301T>G
NM_001453.3:c.*639T>G MANE Select NP_001444.2:n.*639T>G