Canonical Allele Identifier: CA1605822448
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610687A= , CM000668.2:g.1610687A= GRCh38
NC_000006.11:g.1610922A= , CM000668.1:g.1610922A= GRCh37
NC_000006.10:g.1555921A= NCBI36
NG_009368.1:g.5242A=

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.242A= MANE Select ENSP00000493906.1:p.Tyr81=
ENST00000380874.3:c.242A= ENSP00000370256.2:p.Tyr81=
NM_001453.2:c.242A= NP_001444.2:p.Tyr81=
NM_001453.3:c.242A= MANE Select NP_001444.2:p.Tyr81=