Canonical Allele Identifier: CA2677061074
Gene: FOXC1 HGNC NCBI

Linked Data

gnomAD v4: 6-1612776-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612776G>T , CM000668.2:g.1612776G>T GRCh38
NC_000006.11:g.1613011G>T , CM000668.1:g.1613011G>T GRCh37
NC_000006.10:g.1558010G>T NCBI36
NG_009368.1:g.7331G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*669G>T MANE Select ENSP00000493906.1:n.*669G>T
ENST00000380874.3:c.*669G>T ENSP00000370256.2:n.*669G>T
NM_001453.2:c.2331G>T NP_001444.2:n.2331G>T
NM_001453.3:c.*669G>T MANE Select NP_001444.2:n.*669G>T