Canonical Allele Identifier: CA565018175
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1487002586
gnomAD v2: 6-1610253-C-T
gnomAD v3: 6-1610018-C-T
gnomAD v4: 6-1610018-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610018C>T , CM000668.2:g.1610018C>T GRCh38
NC_000006.11:g.1610253C>T , CM000668.1:g.1610253C>T GRCh37
NC_000006.10:g.1555252C>T NCBI36
NG_009368.1:g.4573C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.-428C>T MANE Select ENSP00000493906.1:n.-428C>T
ENST00000380874.3:c.-428C>T ENSP00000370256.2:n.-428C>T
NM_001453.3:c.-428C>T MANE Select NP_001444.2:n.-428C>T