Canonical Allele Identifier: CA2677060915
Gene: FOXC1 HGNC NCBI

Linked Data

gnomAD v4: 6-1612457-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612457C>T , CM000668.2:g.1612457C>T GRCh38
NC_000006.11:g.1612692C>T , CM000668.1:g.1612692C>T GRCh37
NC_000006.10:g.1557691C>T NCBI36
NG_009368.1:g.7012C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*350C>T MANE Select ENSP00000493906.1:n.*350C>T
ENST00000380874.3:c.*350C>T ENSP00000370256.2:n.*350C>T
NM_001453.2:c.2012C>T NP_001444.2:n.2012C>T
NM_001453.3:c.*350C>T MANE Select NP_001444.2:n.*350C>T