Canonical Allele Identifier: CA1605821825
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1609919A= , CM000668.2:g.1609919A= GRCh38
NC_000006.11:g.1610154A= , CM000668.1:g.1610154A= GRCh37
NC_000006.10:g.1555153A= NCBI36
NG_009368.1:g.4474A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-527A= MANE Select ENSP00000493906.1:n.-527A=
NM_001453.3:c.-527A= MANE Select NP_001444.2:n.-527A=