Canonical Allele Identifier: CA1605821917
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610008G= , CM000668.2:g.1610008G= GRCh38
NC_000006.11:g.1610243G= , CM000668.1:g.1610243G= GRCh37
NC_000006.10:g.1555242G= NCBI36
NG_009368.1:g.4563G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-438G= MANE Select ENSP00000493906.1:n.-438G=
ENST00000380874.3:c.-438G= ENSP00000370256.2:n.-438G=
NM_001453.3:c.-438G= MANE Select NP_001444.2:n.-438G=