Canonical Allele Identifier: CA2769749162
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612675C>T , CM000668.2:g.1612675C>T GRCh38
NC_000006.11:g.1612910C>T , CM000668.1:g.1612910C>T GRCh37
NC_000006.10:g.1557909C>T NCBI36
NG_009368.1:g.7230C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.*568C>T MANE Select ENSP00000493906.1:n.*568C>T
ENST00000380874.3:c.*568C>T ENSP00000370256.2:n.*568C>T
NM_001453.2:c.2230C>T NP_001444.2:n.2230C>T
NM_001453.3:c.*568C>T MANE Select NP_001444.2:n.*568C>T