Canonical Allele Identifier: CA2677061100
Gene: FOXC1 HGNC NCBI

Linked Data

gnomAD v4: 6-1612875-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612875G>T , CM000668.2:g.1612875G>T GRCh38
NC_000006.11:g.1613110G>T , CM000668.1:g.1613110G>T GRCh37
NC_000006.10:g.1558109G>T NCBI36
NG_009368.1:g.7430G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.*768G>T MANE Select ENSP00000493906.1:n.*768G>T
ENST00000380874.3:c.*768G>T ENSP00000370256.2:n.*768G>T
NM_001453.2:c.2430G>T NP_001444.2:n.2430G>T
NM_001453.3:c.*768G>T MANE Select NP_001444.2:n.*768G>T