Canonical Allele Identifier: CA362558722
Gene: FOXC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610840T>A , CM000668.2:g.1610840T>A GRCh38
NC_000006.11:g.1611075T>A , CM000668.1:g.1611075T>A GRCh37
NC_000006.10:g.1556074T>A NCBI36
NG_009368.1:g.5395T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.395T>A MANE Select ENSP00000493906.1:p.Leu132His
ENST00000380874.3:c.395T>A ENSP00000370256.2:p.Leu132His
NM_001453.2:c.395T>A NP_001444.2:p.Leu132His
NM_001453.3:c.395T>A MANE Select NP_001444.2:p.Leu132His